SDTMIG v3.3 scraping for specifications

Role,Dataset Name,Variable Name,Variable Label,Type,Variable Name (no prefix),CDISC Notes,Seq. for Order,Observation Class,Core,"Controlled Terms, Codelist or Format",Domain Prefix,Variable \n Label
Identifier,CO,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Special-Purpose,Req,,,
Identifier,CO,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Special-Purpose,Req,CO,,
Record Qualifier,CO,RDOMAIN,Related Domain Abbreviation,Char,RDOMAIN,Two-character abbreviation for the domain of the parent record(s). Null for comments collected on a general comments or additional information CRF page.,3,Special-Purpose,Perm,,,
Identifier,CO,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product.,4,Special-Purpose,Req,,,
Identifier,CO,COSEQ,Sequence Number,Num,SEQ,Sequence Number given to ensure uniqueness of subject records within a domain. May be any valid number.,5,Special-Purpose,Req,,CO,
Record Qualifier,CO,IDVAR,Identifying Variable,Char,IDVAR,Identifying variable in the parent dataset that identifies the record(s) to which the comment applies. Examples AESEQ or CMGRPID. Used only when individual comments are related to domain records. Null for comments collected on separate CRFs.,6,Special-Purpose,Perm,,,
Record Qualifier,CO,IDVARVAL,Identifying Variable Value,Char,IDVARVAL,Value of identifying variable of the parent record(s). Used only when individual comments are related to domain records. Null for comments collected on separate CRFs.,7,Special-Purpose,Perm,,,
Record Qualifier,CO,COREF,Comment Reference,Char,REF,"Sponsor-defined reference associated with the comment. May be the CRF page number (e.g., 650), or a module name (e.g., DEMOG), or a combination of information that identifies the reference (e.g. 650-VITALS-VISIT 2).",8,Special-Purpose,Perm,,CO,
Topic,CO,COVAL,Comment,Char,VAL,The text of the comment. Text over 200 characters can be added to additional columns COVAL1-COVALn. See Assumption 3.,9,Special-Purpose,Req,,CO,
Record Qualifier,CO,COEVAL,Evaluator,Char,EVAL,"Used to describe the originator of the comment. Examples: CENTRAL, REVIEWER, ADJUDICATION COMMITTEE, PRINCIPAL INVESTIGATOR.",10,Special-Purpose,Perm,,CO,
Record Qualifier,CO,COEVALID,Evaluator Identifier,Char,EVALID,"Used to distinguish multiple evaluators with the same role recorded in --EVAL. Examples: RADIOLOGIST, RADIOLOGIST1, RADIOLOGIST2.",11,Special-Purpose,Perm,(MEDEVAL),CO,
Timing,CO,CODTC,Date/Time of Comment,Char,DTC,Date/time of comment on dedicated comment form. Should be null if this is a child record of another domain or if comment date was not collected.,12,Special-Purpose,Perm,ISO 8601,CO,
Timing,CO,CODY,Study Day of Comment,Num,DY,"Study day of the comment, in integer days. The algorithm for calculations must be relative to the sponsor-defined RFSTDTC variable in the Demographics (DM) domain.",13,Special-Purpose,Perm,,CO,
Identifier,DM,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Special-Purpose,Req,,,
Identifier,DM,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Special-Purpose,Req,DM,,
Identifier,DM,USUBJID,Unique Subject Identifier,Char,USUBJID,"Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product. This must be a unique number, and could be a compound identifier formed by concatenating STUDYID-SITEID-SUBJID.",3,Special-Purpose,Req,,,
Topic,DM,SUBJID,Subject Identifier for the Study,Char,SUBJID,"Subject identifier, which must be unique within the study. Often the ID of the subject as recorded on a CRF.",4,Special-Purpose,Req,,,
Record Qualifier,DM,RFSTDTC,Subject Reference Start Date/Time,Char,RFSTDTC,Reference Start Date/time for the subject in ISO 8601 character format. Usually equivalent to date/time when subject was first exposed to study treatment. See Assumption 9 for additional detail on when RFSTDTC may be null.,5,Special-Purpose,Exp,ISO 8601,,
Record Qualifier,DM,RFENDTC,Subject Reference End Date/Time,Char,RFENDTC,"Reference End Date/time for the subject in ISO 8601 character format. Usually equivalent to the date/time when subject was determined to have ended the trial, and often equivalent to date/time of last exposure to study treatment. Required for all randomized subjects; null for screen failures or unassigned subjects.",6,Special-Purpose,Exp,ISO 8601,,
Record Qualifier,DM,RFXSTDTC,Date/Time of First Study Treatment,Char,RFXSTDTC,"First date/time of exposure to any protocol-specified treatment or therapy, equal to the earliest value of EXSTDTC.",7,Special-Purpose,Exp,ISO 8601,,
Record Qualifier,DM,RFXENDTC,Date/Time of Last Study Treatment,Char,RFXENDTC,"Last date/time of exposure to any protocol-specified treatment or therapy, equal to the latest value of EXENDTC (or the latest value of EXSTDTC if EXENDTC was not collected or is missing).",8,Special-Purpose,Exp,ISO 8601,,
Record Qualifier,DM,RFICDTC,Date/Time of Informed Consent,Char,RFICDTC,"Date/time of informed consent in ISO 8601 character format. This will be the same as the date of informed consent in the Disposition domain, if that protocol milestone is documented. Would be null only in studies not collecting the date of informed consent.",9,Special-Purpose,Exp,ISO 8601,,
Record Qualifier,DM,RFPENDTC,Date/Time of End of Participation,Char,RFPENDTC,"Date/time when subject ended participation or follow-up in a trial, as defined in the protocol, in ISO 8601 character format. Should correspond to the last known date of contact. Examples include completion date, withdrawal date, last follow-up, date recorded for lost to follow up, or death date.",10,Special-Purpose,Exp,ISO 8601,,
Record Qualifier,DM,DTHDTC,Date/Time of Death,Char,DTHDTC,"Date/time of death for any subject who died, in ISO 8601 format. Should represent the date/time that is captured in the clinical-trial database.",11,Special-Purpose,Exp,ISO 8601,,
Record Qualifier,DM,DTHFL,Subject Death Flag,Char,DTHFL,Indicates the subject died. Should be "Y" or null. Should be populated even when the death date is unknown.,12,Special-Purpose,Exp,(NY),,
Record Qualifier,DM,SITEID,Study Site Identifier,Char,SITEID,Unique identifier for a site within a study.,13,Special-Purpose,Req,,,
Record Qualifier,DM,INVID,Investigator Identifier,Char,INVID,An identifier to describe the Investigator for the study. May be used in addition to SITEID. Not needed if SITEID is equivalent to INVID.,14,Special-Purpose,Perm,,,
Synonym Qualifier,DM,INVNAM,Investigator Name,Char,INVNAM,Name of the investigator for a site.,15,Special-Purpose,Perm,,,
Record Qualifier,DM,BRTHDTC,Date/Time of Birth,Char,BRTHDTC,Date/time of birth of the subject.,16,Special-Purpose,Perm,ISO 8601,,
Record Qualifier,DM,AGE,Age,Num,AGE,"Age expressed in AGEU. May be derived from RFSTDTC and BRTHDTC, but BRTHDTC may not be available in all cases (due to subject privacy concerns).",17,Special-Purpose,Exp,,,
Variable Qualifier,DM,AGEU,Age Units,Char,AGEU,Units associated with AGE.,18,Special-Purpose,Exp,(AGEU),,
Record Qualifier,DM,SEX,Sex,Char,SEX,Sex of the subject.,19,Special-Purpose,Req,(SEX),,
Record Qualifier,DM,RACE,Race,Char,RACE,"Race of the subject. Sponsors should refer to ""Collection of Race and Ethnicity Data in Clinical Trials"" (FDA, October, 2016) for guidance regarding the collection of race (https://www.fda.gov/downloads/regulatoryinformation/guidances/ucm126396.pdf) See Assumption below regarding RACE.",20,Special-Purpose,Exp,(RACE),,
Record Qualifier,DM,ETHNIC,Ethnicity,Char,ETHNIC,"The ethnicity of the subject. Sponsors should refer to ""Collection of Race and Ethnicity Data in Clinical Trials"" (FDA, October, 2016) for guidance regarding the collection of ethnicity (https://www.fda.gov/downloads/regulatoryinformation/guidances/ucm126396.pdf).",21,Special-Purpose,Perm,(ETHNIC),,
Record Qualifier,DM,ARMCD,Planned Arm Code,Char,ARMCD,"ARMCD is limited to 20 characters. It is not subject to the character restrictions that apply to TESTCD.The maximum length of ARMCD is longer than for other ""short"" variables to accommodate the kind of values that are likely to be needed for crossover trials. For example, if ARMCD values for a seven-period crossover were constructed using two-character abbreviations for each treatment and separating hyphens, the length of ARMCD values would be 20. If the subject was not assigned to an Arm, ARMCD is null and ARMNRS is populated. \n With the exception of studies which use multi-stage Arm assignments, must be a value of ARMCD in the Trial Arms Dataset.",22,Special-Purpose,Exp,,,
Synonym Qualifier,DM,ARM,Description of Planned Arm,Char,ARM,"Name of the Arm to which the subject was assigned. If the subject was not assigned to an Arm, ARM is null and ARMNRS is populated. \n With the exception of studies which use multi-stage Arm assignments, must be a value of ARM in the Trial Arms Dataset.",23,Special-Purpose,Exp,,,
Record Qualifier,DM,ACTARMCD,Actual Arm Code,Char,ACTARMCD,"Code of actual Arm. ACTARMCD is limited to 20 characters. It is not subject to the character restrictions that apply to TESTCD. The maximum length of ACTARMCD is longer than for other short variables to accommodate the kind of values that are likely to be needed for crossover trials. \n With the exception of studies which use multi-stage Arm assignments, must be a value of ARMCD in the Trial Arms Dataset. \n If the subject was not assigned to an Arm or followed a course not described by any planned Arm, ACTARMCD is null and ARMNRS is populated.",24,Special-Purpose,Exp,,,
Synonym Qualifier,DM,ACTARM,Description of Actual Arm,Char,ACTARM,"Description of actual Arm. \n With the exception of studies which use multi-stage Arm assignments, must be a value of ARM in the Trial Arms Dataset. \n If the subject was not assigned to an Arm or followed a course not described by any planned Arm, ACTARM is null and ARMNRS is populated.",25,Special-Purpose,Exp,,,
Record Qualifier,DM,ARMNRS,Reason Arm and/or Actual Arm is Null,Char,ARMNRS,"A coded reason that Arm variables (ARM and ARMCD) and/or actual Arm variables (ACTARM and ACTARMCD) are null. Examples: ""SCREEN FAILURE"", ""NOT ASSIGNED"", ""ASSIGNED, NOT TREATED"", ""UNPLANNED TREATMENT"". It is assumed that if the Arm and actual Arm variables are null, the same reason applies to both Arm and actual Arm.",26,Special-Purpose,Exp,,,
Record Qualifier,DM,ACTARMUD,Description of Unplanned Actual Arm,Char,ACTARMUD,A description of actual treatment for a subject who did not receive treatment described in one of the planned trial Arms.,27,Special-Purpose,Exp,,,
Record Qualifier,DM,COUNTRY,Country,Char,COUNTRY,Country of the investigational site in which the subject participated in the trial.,28,Special-Purpose,Req,ISO 3166-1 Alpha-3,,
Timing,DM,DMDTC,Date/Time of Collection,Char,DTC,Date/time of demographic data collection.,29,Special-Purpose,Perm,ISO 8601,DM,
Timing,DM,DMDY,Study Day of Collection,Num,DY,Study day of collection measured as integer days.,30,Special-Purpose,Perm,,DM,
Identifier,SE,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Special-Purpose,Req,,,
Identifier,SE,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Special-Purpose,Req,SE,,
Identifier,SE,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product.,3,Special-Purpose,Req,,,
Identifier,SE,SESEQ,Sequence Number,Num,SEQ,Sequence number given to ensure uniqueness of subject records within a domain. Should be assigned to be consistent chronological order.,4,Special-Purpose,Req,,SE,
Topic,SE,ETCD,Element Code,Char,ETCD,"1. ETCD (the companion to ELEMENT) is limited to 8 characters and does not have special character restrictions. These values should be short for ease of use in programming, but it is not expected that ETCD will need to serve as a variable name. \n 2. If an encountered Element differs from the planned Element to the point that it is considered a new Element, then use "UNPLAN" as the value for ETCD to represent this Element.",5,Special-Purpose,Req,,,
Synonym Qualifier,SE,ELEMENT,Description of Element,Char,ELEMENT,The name of the Element. If ETCD has a value of "UNPLAN" then ELEMENT should be null.,6,Special-Purpose,Perm,,,
Timing,SE,TAETORD,Planned Order of Element within Arm,Num,TAETORD,Number that gives the planned order of the Element within the subject's assigned Arm.,7,Special-Purpose,Perm,,,
Timing,SE,EPOCH,Epoch,Char,EPOCH,Epoch associated with the Element in the planned sequence of Elements for the Arm to which the subject was assigned.,8,Special-Purpose,Perm,(EPOCH),,
Timing,SE,SESTDTC,Start Date/Time of Element,Char,STDTC,Start date/time for an Element for each subject.,9,Special-Purpose,Req,ISO 8601,SE,
Timing,SE,SEENDTC,End Date/Time of Element,Char,ENDTC,End date/time for an Element for each subject.,10,Special-Purpose,Exp,ISO 8601,SE,
Synonym Qualifier,SE,SEUPDES,Description of Unplanned Element,Char,UPDES,Description of what happened to the subject during an unplanned Element. Used only if ETCD has the value of "UNPLAN".,11,Special-Purpose,Perm,,SE,
Identifier,SM,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Special-Purpose,Req,,,
Identifier,SM,DOMAIN,Domain,Char,DOMAIN,Two-character abbreviation for the domain.,2,Special-Purpose,Req,SM,,
Identifier,SM,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across all studies.,3,Special-Purpose,Req,,,
Identifier,SM,SMSEQ,Sequence Number,Num,SEQ,Sequence number to ensure uniqueness of subject records. Should be assigned to be consistent chronological order.,4,Special-Purpose,Req,,SM,
Topic,SM,MIDS,Disease Milestone Instance Name,Char,MIDS,"Name of the specific Disease Milestone. For types of Disease Milestone that can occur multiple times, the name will end with a sequence number. Example: ""HYPO1"".",5,Special-Purpose,Req,,,
Record Qualifier,SM,MIDSTYPE,Disease Milestone Type,Char,MIDSTYPE,The type of Disease Milestone. Example: "HYPOGLYCEMIC EVENT".,6,Special-Purpose,Req,,,
Timing,SM,SMSTDTC,Start Date/Time of Milestone,Char,STDTC,"State date/time of Milestone Instance, if Milestone is an intervention or event, or date of Milestone if Milestone is a finding.",7,Special-Purpose,Exp,ISO 8601,SM,
Timing,SM,SMENDTC,End Date/Time of Milestone,Char,ENDTC,End date/time of Disease Milestone Instance.,8,Special-Purpose,Exp,ISO 8601,SM,
Timing,SM,SMSTDY,Study Day of Start of Milestone,Num,STDY,"Study day of start of Disease Milestone Instance, relative to the sponsor-defined RFSTDTC.",9,Special-Purpose,Exp,,SM,
Timing,SM,SMENDY,Study Day of End of Milestone,Num,ENDY,"Study day of end of Disease Milestone Instance, relative to the sponsor-defined RFSTDTC.",10,Special-Purpose,Exp,,SM,
Identifier,SV,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Special-Purpose,Req,,,
Identifier,SV,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Special-Purpose,Req,SV,,
Identifier,SV,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product.,3,Special-Purpose,Req,,,
Topic,SV,VISITNUM,Visit Number,Num,VISITNUM,"1. Clinical encounter number. (Decimal numbering may be useful for inserting unplanned visits.) \n 2. Numeric version of VISIT, used for sorting.",4,Special-Purpose,Req,,,
Synonym Qualifier,SV,VISIT,Visit Name,Char,VISIT,Protocol-defined description of clinical encounter.May be used in addition to VISITNUM and/or VISITDY as a text description of the clinical encounter.,5,Special-Purpose,Perm,,,
Timing,SV,VISITDY,Planned Study Day of Visit,Num,VISITDY,Planned study day of the start of the visit based upon RFSTDTC in Demographics.,6,Special-Purpose,Perm,,,
Timing,SV,SVSTDTC,Start Date/Time of Visit,Char,STDTC,Start date/time for a Visit.,7,Special-Purpose,Exp,ISO 8601,SV,
Timing,SV,SVENDTC,End Date/Time of Visit,Char,ENDTC,End date/time of a Visit.,8,Special-Purpose,Exp,ISO 8601,SV,
Timing,SV,SVSTDY,Study Day of Start of Visit,Num,STDY,Study day of start of visit relative to the sponsor-defined RFSTDTC.,9,Special-Purpose,Perm,,SV,
Timing,SV,SVENDY,Study Day of End of Visit,Num,ENDY,Study day of end of visit relative to the sponsor-defined RFSTDTC.,10,Special-Purpose,Perm,,SV,
Synonym Qualifier,SV,SVUPDES,Description of Unplanned Visit,Char,UPDES,Description of what happened to the subject during an unplanned visit.,11,Special-Purpose,Perm,,SV,
Identifier,AG,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Interventions,Req,,,
Identifier,AG,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Interventions,Req,AG,,
Identifier,AG,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product.,3,Interventions,Req,,,
Identifier,AG,AGSEQ,Sequence Number,Num,SEQ,Sequence Number given to ensure uniqueness of subject records within a domain. May be any valid number.,4,Interventions,Req,,AG,
Identifier,AG,AGGRPID,Group ID,Char,GRPID,Used to tie together a block of related records in a single domain for a subject.,5,Interventions,Perm,,AG,
Identifier,AG,AGSPID,Sponsor-Defined Identifier,Char,SPID,Sponsor-defined reference number. Perhaps pre-printed on the CRF as an explicit line identifier or defined in the sponsor's operational database. Example: Line number from the procedure or test page.,6,Interventions,Perm,,AG,
Identifier,AG,AGLNKID,Link ID,Char,LNKID,Identifier used to link related records across domains.This may be a one-to-one or a one-to-many relationship.,7,Interventions,Perm,,AG,
Identifier,AG,AGLNKGRP,Link Group ID,Char,LNKGRP,Identifier used to link related records across domains.This will usually be a many-to-one relationship.,8,Interventions,Perm,,AG,
Topic,AG,AGTRT,Reported Agent Name,Char,TRT,Verbatim medication name that is either pre-printed or collected on a CRF.,9,Interventions,Req,,AG,
Synonym Qualifier,AG,AGMODIFY,Modified Reported Name,Char,MODIFY,"If AGTRT is modified to facilitate coding, then AGMODIFY will contain the modified text.",10,Interventions,Perm,,AG,
Synonym Qualifier,AG,AGDECOD,Standardized Agent Name,Char,DECOD,"Standardized or dictionary-derived text description of AGTRT or AGMODIFY. Equivalent to the generic medication name in WHO Drug. The sponsor is expected to provide the dictionary name and version used to map the terms utilizing the external codelist element in the Define-XML document. If an intervention term does not have a decode value in the dictionary, then AGDECOD will be left blank.",11,Interventions,Perm,,AG,
Grouping Qualifier,AG,AGCAT,Category for Agent,Char,CAT,"Used to define a category of agent. Examples: "CHALLENGE AGENT", or "PET TRACER".",12,Interventions,Perm,,AG,
Grouping Qualifier,AG,AGSCAT,Subcategory for Agent,Char,SCAT,Further categorization of agent.,13,Interventions,Perm,,AG,
Variable Qualifier,AG,AGPRESP,AG Pre-Specified,Char,PRESP,Used to indicate whether ("Y"/null) information about the use of a specific agent was solicited on the CRF.,14,Interventions,Perm,(NY),AG,
Record Qualifier,AG,AGOCCUR,AG Occurrence,Char,OCCUR,"When the use of specific agent is solicited, AGOCCUR is used to indicate whether or not ("Y"/"N") use of the agent occurred. Values are null for agents not specifically solicited.",15,Interventions,Perm,(NY),AG,
Record Qualifier,AG,AGSTAT,Completion Status,Char,STAT,Used to indicate that a question about a pre-specified agent was not answered. Should be null or have a value of "NOT DONE".,16,Interventions,Perm,(ND),AG,
Record Qualifier,AG,AGREASND,Reason Procedure Agent Not Collected,Char,REASND,Describes the reason a response to a question about the occurrence of a procedure agent was not collected. Used in conjunction with AGSTAT when value is "NOT DONE".,17,Interventions,Perm,,AG,
Variable Qualifier,AG,AGCLAS,Agent Class,Char,CLAS,"Drug class. May be obtained from coding. When coding to a single class, populate with class value. If using a dictionary and coding to multiple classes, then follow assumption 4.1.2.8.3 or omit AGCLAS.",18,Interventions,Perm,,AG,
Variable Qualifier,AG,AGCLASCD,Agent Class Code,Char,CLASCD,"Class code corresponding to AGCLAS. Drug class. May be obtained from coding. When coding to a single class, populate with class code. If using a dictionary and coding to multiple classes, then follow Assumption 4.1.2.8.3, Multiple Values for a Non-Result Qualifier Variable, or omit AGCLASCD.",19,Interventions,Perm,,AG,
Record Qualifier,AG,AGDOSE,Dose per Administration,Num,DOSE,Amount of AGTRT taken.,20,Interventions,Perm,,AG,
Record Qualifier,AG,AGDOSTXT,Dose Description,Char,DOSTXT,"Dosing amounts or a range of dosing information collected in text form. Units may be stored in AGDOSU. Example: "200-400", "15-20".",21,Interventions,Perm,,AG,
Variable Qualifier,AG,AGDOSU,Dose Units,Char,DOSU,"Units for AGDOSE and AGDOSTXT. Examples: "ng", "mg", or "mg/kg".",22,Interventions,Perm,(UNIT),AG,
Variable Qualifier,AG,AGDOSFRM,Dose Form,Char,DOSFRM,"Dose form for AGTRT. Examples: "TABLET", "AEROSOL".",23,Interventions,Perm,(FRM),AG,
Variable Qualifier,AG,AGDOSFRQ,Dosing Frequency per Interval,Char,DOSFRQ,Usually expressed as the number of repeated administrations of AGDOSE within a specific time period. Example: "ONCE".,24,Interventions,Perm,(FREQ),AG,
Variable Qualifier,AG,AGROUTE,Route of Administration,Char,ROUTE,Route of administration for AGTRT. Examples: "ORAL".,25,Interventions,Perm,(ROUTE),AG,
Timing,AG,VISITNUM,Visit Number,Num,VISITNUM,"1. Clinical encounter number. \n 2. Numeric version of VISIT, used for sorting.",26,Interventions,Exp,,,
Timing,AG,VISIT,Visit Name,Char,VISIT,Protocol-defined description of clinical encounter.May be used in addition to VISITNUM and/or VISITDY.,27,Interventions,Perm,,,
Timing,AG,VISITDY,Planned Study Day of Visit,Num,VISITDY,Planned study day of the visit based upon RFSTDTC in Demographics.,28,Interventions,Perm,,,
Timing,AG,TAETORD,Planned Order of Element within Arm,Num,TAETORD,Number that gives the planned order of the Element within the Arm for the Element in which the agent administration started.,29,Interventions,Perm,,,
Timing,AG,EPOCH,Epoch,Char,EPOCH,Epoch associated with the start date/time of the agent administration started.,30,Interventions,Perm,(EPOCH),,
Timing,AG,AGSTDTC,Start Date/Time of Agent,Char,STDTC,The date/time when administration of the treatment indicated by AGTRT and the dosing variables began.,31,Interventions,Perm,ISO 8601,AG,
Timing,AG,AGENDTC,End Date/Time of Agent,Char,ENDTC,The date/time when administration of the treatment indicated by AGTRT and the dosing variables ended.,32,Interventions,Perm,ISO 8601,AG,
Timing,AG,AGSTDY,Study Day of Start of Agent,Num,STDY,Study day of start of agent relative to the sponsor-defined RFSTDTC.,33,Interventions,Perm,,AG,
Timing,AG,AGENDY,Study Day of End of Agent,Num,ENDY,Study day of end of agent relative to the sponsor-defined RFSTDTC.,34,Interventions,Perm,,AG,
Timing,AG,AGDUR,Duration of Agent,Char,DUR,Collected duration for an agent episode. Used only if collected on the CRF and not derived from start and end date/times.,35,Interventions,Perm,ISO 8601,AG,
Timing,AG,AGSTRF,Start Relative to Reference Period,Char,STRF,"Describes the start of the agent relative to sponsor-defined reference period. The sponsor-defined reference period is a continuous period of time defined by a discrete starting point and a discrete ending point (represented by RFSTDTC and RFENDTC in Demographics). If information such as "PRIOR", "ONGOING", or "CONTINUING" was collected, this information may be translated into AGSTRF.",36,Interventions,Perm,(STENRF),AG,
Timing,AG,AGENRF,End Relative to Reference Period,Char,ENRF,"Describes the end of the agent relative to the sponsor-defined reference period. The sponsor-defined reference period is a continuous period of time defined by a discrete starting point and a discrete ending point (represented by RFSTDTC and RFENDTC in Demographics). If information such as "PRIOR", "ONGOING", or "CONTINUING" was collected, this information may be translated into AGENRF.",37,Interventions,Perm,(STENRF),AG,
Timing,AG,AGSTRTPT,Start Relative to Reference Time Point,Char,STRTPT,Identifies the start of the agent as being before or after the sponsor-defined reference time point defined by variable AGSTTPT.,38,Interventions,Perm,(STENRF),AG,
Timing,AG,AGSTTPT,Start Reference Time Point,Char,STTPT,Description or date/time in ISO 8601 character format of the reference point referred to by AGSTRTPT. Examples: "2003-12-15" or "VISIT 1".,39,Interventions,Perm,,AG,
Timing,AG,AGENRTPT,End Relative to Reference Time Point,Char,ENRTPT,Identifies the end of the agent as being before or after the reference time point defined by variable AGENTPT. Identifies the end of the agent as being before or after the sponsor-defined reference time point defined by variable AGENTPT.,40,Interventions,Perm,(STENRF),AG,
Timing,AG,AGENTPT,End Reference Time Point,Char,ENTPT,Description or date/time in ISO 8601 character format of the reference point referred to by AGENRTPT. Examples: "2003-12-25" or "VISIT 2".,41,Interventions,Perm,,AG,
Identifier,CM,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Interventions,Req,,,
Identifier,CM,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Interventions,Req,CM,,
Identifier,CM,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product.,3,Interventions,Req,,,
Identifier,CM,CMSEQ,Sequence Number,Num,SEQ,Sequence number to ensure uniqueness of subject records within a domain. May be any valid number.,4,Interventions,Req,,CM,
Identifier,CM,CMGRPID,Group ID,Char,GRPID,Used to tie together a block of related records in a single domain for a subject.,5,Interventions,Perm,,CM,
Identifier,CM,CMSPID,Sponsor-Defined Identifier,Char,SPID,Sponsor-defined reference number. Example: a number pre-printed on the CRF as an explicit line identifier or record identifier defined in the sponsor's operational database. Example: line number on a concomitant medication page.,6,Interventions,Perm,,CM,
Topic,CM,CMTRT,"Reported Name of Drug, Med, or Therapy",Char,TRT,Verbatim medication name that is either pre-printed or collected on a CRF.,7,Interventions,Req,,CM,
Synonym Qualifier,CM,CMMODIFY,Modified Reported Name,Char,MODIFY,"If CMTRT is modified to facilitate coding, then CMMODIFY will contain the modified text.",8,Interventions,Perm,,CM,
Synonym Qualifier,CM,CMDECOD,Standardized Medication Name,Char,DECOD,"Standardized or dictionary-derived text description of CMTRT or CMMODIFY. Equivalent to the generic drug name in WHO Drug. The sponsor is expected to provide the dictionary name and version used to map the terms utilizing the external codelist element in the Define-XML document. If an intervention term does not have a decode value in the dictionary, then CMDECOD will be left blank.",9,Interventions,Perm,,CM,
Grouping Qualifier,CM,CMCAT,Category for Medication,Char,CAT,"Used to define a category of medications/treatment. Examples: ""PRIOR"", ""CONCOMITANT"", ""ANTI-CANCER MEDICATION"", or ""GENERAL CONMED"".",10,Interventions,Perm,,CM,
Grouping Qualifier,CM,CMSCAT,Subcategory for Medication,Char,SCAT,"A further categorization of medications/treatment. Examples: ""CHEMOTHERAPY"", ""HORMONAL THERAPY"", ""ALTERNATIVE THERAPY"".",11,Interventions,Perm,,CM,
Variable Qualifier,CM,CMPRESP,CM Pre-specified,Char,PRESP,Used to indicate whether ("Y"/null) information about the use of a specific medication was solicited on the CRF.,12,Interventions,Perm,(NY),CM,
Record Qualifier,CM,CMOCCUR,CM Occurrence,Char,OCCUR,When the use of a specific medication is solicited. CMOCCUR is used to indicate whether or not ("Y"/"N") use of the medication occurred. Values are null for medications not specifically solicited.,13,Interventions,Perm,(NY),CM,
Record Qualifier,CM,CMSTAT,Completion Status,Char,STAT,Used to indicate that a question about the occurrence of a pre-specified intervention was not answered. Should be null or have a value of "NOT DONE".,14,Interventions,Perm,(ND),CM,
Record Qualifier,CM,CMREASND,Reason Medication Not Collected,Char,REASND,Reason not done. Used in conjunction with CMSTAT when value is "NOT DONE".,15,Interventions,Perm,,CM,
Record Qualifier,CM,CMINDC,Indication,Char,INDC,"Denotes why a medication was taken or administered. Examples: ""NAUSEA"", ""HYPERTENSION"".",16,Interventions,Perm,,CM,
Variable Qualifier,CM,CMCLAS,Medication Class,Char,CLAS,"Drug class. May be obtained from coding. When coding to a single class, populate with class value. If using a dictionary and coding to multiple classes, then follow Section 4.2.8.3, Multiple Values for a Non-Result Qualifier Variable, or omit CMCLAS.",17,Interventions,Perm,,CM,
Variable Qualifier,CM,CMCLASCD,Medication Class Code,Char,CLASCD,"Class code corresponding to CMCLAS. Drug class. May be obtained from coding. When coding to a single class, populate with class code. If using a dictionary and coding to multiple classes, then follow Section 4.2.8.3, Multiple Values for a Non-Result Qualifier Variable, or omit CMCLASCD.",18,Interventions,Perm,,CM,
Record Qualifier,CM,CMDOSE,Dose per Administration,Num,DOSE,Amount of CMTRT given. Not populated when CMDOSTXT is populated.,19,Interventions,Perm,,CM,
Record Qualifier,CM,CMDOSTXT,Dose Description,Char,DOSTXT,"Dosing amounts or a range of dosing information collected in text form. Units may be stored in CMDOSU. Examples: ""200-400"", ""15-20"". Not populated when CMDOSE is populated.",20,Interventions,Perm,,CM,
Variable Qualifier,CM,CMDOSU,Dose Units,Char,DOSU,"Units for CMDOSE, CMDOSTOT, or CMDOSTXT. Examples: ""ng"", ""mg"", or ""mg/kg"".",21,Interventions,Perm,(UNIT),CM,
Variable Qualifier,CM,CMDOSFRM,Dose Form,Char,DOSFRM,"Dose form for CMTRT. Examples: ""TABLET"", ""LOTION"".",22,Interventions,Perm,(FRM),CM,
Variable Qualifier,CM,CMDOSFRQ,Dosing Frequency per Interval,Char,DOSFRQ,"Usually expressed as the number of repeated administrations of CMDOSE within a specific time period. Examples: ""BID"" (twice daily), ""Q12H"" (every 12 hours).",23,Interventions,Perm,(FREQ),CM,
Record Qualifier,CM,CMDOSTOT,Total Daily Dose,Num,DOSTOT,Total daily dose of CMTRT using the units in CMDOSU. Used when dosing is collected as Total Daily Dose. Total dose over a period other than day could be recorded in a separate Supplemental Qualifier variable.,24,Interventions,Perm,,CM,
Variable Qualifier,CM,CMDOSRGM,Intended Dose Regimen,Char,DOSRGM,"Text description of the (intended) schedule or regimen for the Intervention. Example: ""TWO WEEKS ON, TWO WEEKS OFF"".",25,Interventions,Perm,,CM,
Variable Qualifier,CM,CMROUTE,Route of Administration,Char,ROUTE,"Route of administration for the intervention. Examples: ""ORAL"", ""INTRAVENOUS"".",26,Interventions,Perm,(ROUTE),CM,
Record Qualifier,CM,CMADJ,Reason for Dose Adjustment,Char,ADJ,"Describes reason or explanation of why a dose is adjusted. Examples: ""ADVERSE EVENT"", ""INSUFFICIENT RESPONSE"", ""NON-MEDICAL REASON"".",27,Interventions,Perm,,CM,
Record Qualifier,CM,CMRSDISC,Reason the Intervention Was Discontinued,Char,RSDISC,"When dosing of a treatment is recorded over multiple successive records, this variable is applicable only for the (chronologically) last record for the treatment.",28,Interventions,Perm,,CM,
Timing,CM,TAETORD,Planned Order of Element within Arm,Num,TAETORD,Number that gives the planned order of the Element within the Arm for the Element in which the medication administration started. Null for medications that started before study participation.,29,Interventions,Perm,,,
Timing,CM,EPOCH,Epoch,Char,EPOCH,Epoch associated with the start date/time of the medication administration. Null for medications that started before study participation.,30,Interventions,Perm,(EPOCH),,
Timing,CM,CMSTDTC,Start Date/Time of Medication,Char,STDTC,Start date/time of the medication administration represented in ISO 8601 character format.,31,Interventions,Perm,ISO 8601,CM,
Timing,CM,CMENDTC,End Date/Time of Medication,Char,ENDTC,End date/time of the medication administration represented in ISO 8601 character format.,32,Interventions,Perm,ISO 8601,CM,
Timing,CM,CMSTDY,Study Day of Start of Medication,Num,STDY,Study day of start of medication relative to the sponsor-defined RFSTDTC.,33,Interventions,Perm,,CM,
Timing,CM,CMENDY,Study Day of End of Medication,Num,ENDY,Study day of end of medication relative to the sponsor-defined RFSTDTC.,34,Interventions,Perm,,CM,
Timing,CM,CMDUR,Duration,Char,DUR,Collected duration for a treatment episode. Used only if collected on the CRF and not derived from start and end date/times.,35,Interventions,Perm,ISO 8601,CM,
Timing,CM,CMSTRF,Start Relative to Reference Period,Char,STRF,"Describes the start of the medication relative to sponsor-defined reference period. The sponsor-defined reference period is a continuous period of time defined by a discrete starting point and a discrete ending point (represented by RFSTDTC and RFENDTC in Demographics). If information such as ""PRIOR"" was collected, this information may be translated into CMSTRF. \n Not all values of the codelist are allowable for this variable. See Section 4.4.7, Use of Relative Timing Variables.",36,Interventions,Perm,(STENRF),CM,
Timing,CM,CMENRF,End Relative to Reference Period,Char,ENRF,"Describes the end of the medication relative to the sponsor-defined reference period. The sponsor-defined reference period is a continuous period of time defined by a discrete starting point and a discrete ending point (represented by RFSTDTC and RFENDTC in Demographics). If information such as ""PRIOR"", ""ONGOING, or ""CONTINUING"" was collected, this information may be translated into CMENRF. \n Not all values of the codelist are allowable for this variable. See Section 4.4.7, Use of Relative Timing Variables.",37,Interventions,Perm,(STENRF),CM,
Timing,CM,CMSTRTPT,Start Relative to Reference Time Point,Char,STRTPT,"Identifies the start of the medication as being before or after the sponsor-defined reference time point defined by variable CMSTTPT. \n Not all values of the codelist are allowable for this variable. See Section 4.4.7, Use of Relative Timing Variables.",38,Interventions,Perm,(STENRF),CM,
Timing,CM,CMSTTPT,Start Reference Time Point,Char,STTPT,Description or date/time in ISO 8601 character format of the sponsor-defined reference point referred to by CMSTRTPT. Examples: "2003-12-15" or "VISIT 1".,39,Interventions,Perm,,CM,
Timing,CM,CMENRTPT,End Relative to Reference Time Point,Char,ENRTPT,"Identifies the end of the medication as being before or after the sponsor-defined reference time point defined by variable CMENTPT. \n Not all values of the codelist are allowable for this variable. See Section 4.4.7, Use of Relative Timing Variables.",40,Interventions,Perm,(STENRF),CM,
Timing,CM,CMENTPT,End Reference Time Point,Char,ENTPT,Description or date/time in ISO 8601 character format of the sponsor-defined reference point referred to by CMENRTPT. Examples: "2003-12-25" or "VISIT 2".,41,Interventions,Perm,,CM,
Identifier,EC,STUDYID,,Char,STUDYID,Unique identifier for a study.,1,Interventions,Req,,,Study Identifier
Identifier,EC,DOMAIN,,Char,DOMAIN,Two-character abbreviation for the domain.,2,Interventions,Req,EC,,Domain Abbreviation
Identifier,EC,USUBJID,,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product.,3,Interventions,Req,,,Unique Subject Identifier
Identifier,EC,ECSEQ,,Num,SEQ,Sequence Number given to ensure uniqueness of subject records within a domain. May be any valid number.,4,Interventions,Req,,EC,Sequence Number
Identifier,EC,ECGRPID,,Char,GRPID,Used to tie together a block of related records in a single domain for a subject.,5,Interventions,Perm,,EC,Group ID
Identifier,EC,ECREFID,,Char,REFID,"Internal or external identifier (e.g., kit number, bottle label, vial identifier).",6,Interventions,Perm,,EC,Reference ID
Identifier,EC,ECSPID,,Char,SPID,Sponsor-defined reference number. Perhaps pre-printed on the CRF as an explicit line identifier or defined in the sponsor's operational database. Example: Line number on a CRF Page.,7,Interventions,Perm,,EC,Sponsor-Defined Identifier
Identifier,EC,ECLNKID,,Char,LNKID,Identifier used to link related records across domains.,8,Interventions,Perm,,EC,Link ID
Identifier,EC,ECLNKGRP,,Char,LNKGRP,"Identifier used to link related, grouped records across domains.",9,Interventions,Perm,,EC,Link Group ID
Topic,EC,ECTRT,,Char,TRT,Name of the intervention treatment known to the subject and/or administrator.,10,Interventions,Req,,EC,Name of Treatment
Record Qualifier,EC,ECMOOD,,Char,MOOD,"Mode or condition of the record specifying whether the intervention (activity) is intended to happen or has happened. Values align with BRIDG pillars (e.g., scheduled context, performed context) and HL7 activity moods (e.g., intent, event). Examples: ""SCHEDULED"", ""PERFORMED"".",11,Interventions,Perm,(BRDGMOOD),EC,Mood
Grouping Qualifier,EC,ECCAT,,Char,CAT,Used to define a category of related ECTRT values.,12,Interventions,Perm,,EC,Category of Treatment
Grouping Qualifier,EC,ECSCAT,,Char,SCAT,A further categorization of ECCAT values.,13,Interventions,Perm,,EC,Subcategory of Treatment
Variable Qualifier,EC,ECPRESP,,Char,PRESP,Used when a specific intervention is pre-specified. Values should be "Y" or null.,14,Interventions,Perm,(NY),EC,Pre-Specified
Record Qualifier,EC,ECOCCUR,,Char,OCCUR,"Used to indicate whether a treatment occurred when information about the occurrence is solicited. ECOCCUR = ""N"" when a treatment was not taken, not given, or missed.",15,Interventions,Perm,(NY),EC,Occurrence
Record Qualifier,EC,ECDOSE,,Num,DOSE,Amount of ECTRT when numeric. Not populated when ECDOSTXT is populated.,16,Interventions,Exp,,EC,Dose
Record Qualifier,EC,ECDOSTXT,,Char,DOSTXT,Amount of ECTRT when non-numeric. Dosing amounts or a range of dosing information collected in text form. Example: "200-400". Not populated when ECDOSE is populated.,17,Interventions,Perm,,EC,Dose Description
Variable Qualifier,EC,ECDOSU,,Char,DOSU,"Units for ECDOSE, ECDOSTOT, or ECDOSTXT.",18,Interventions,Exp,(UNIT),EC,Dose Units
Variable Qualifier,EC,ECDOSFRM,,Char,DOSFRM,"Dose form for ECTRT. Examples: ""TABLET"", ""LOTION"".",19,Interventions,Exp,(FRM),EC,Dose Form
Variable Qualifier,EC,ECDOSFRQ,,Char,DOSFRQ,"Usually expressed as the number of repeated administrations of ECDOSE within a specific time period. Examples: ""Q2H"", ""QD"", ""BID"".",20,Interventions,Perm,(FREQ),EC,Dosing Frequency per Interval
Record Qualifier,EC,ECDOSTOT,,Num,DOSTOT,Total daily dose of ECTRT using the units in ECDOSU. Used when dosing is collected as Total Daily Dose.,21,Interventions,Perm,,EC,Total Daily Dose
Variable Qualifier,EC,ECDOSRGM,,Char,DOSRGM,"Text description of the intended schedule or regimen for the Intervention. Example: ""TWO WEEKS ON"", ""TWO WEEKS OFF"".",22,Interventions,Perm,,EC,Intended Dose Regimen
Variable Qualifier,EC,ECROUTE,,Char,ROUTE,"Route of administration for the intervention. Examples: ""ORAL"", ""INTRAVENOUS"".",23,Interventions,Perm,(ROUTE),EC,Route of Administration
Record Qualifier,EC,ECLOT,,Char,LOT,Lot Number of the ECTRT product.,24,Interventions,Perm,,EC,Lot Number
Record Qualifier,EC,ECLOC,,Char,LOC,"Specifies location of administration. Example: ""ARM"", ""LIP"".",25,Interventions,Perm,(LOC),EC,Location of Dose Administration
Variable Qualifier,EC,ECLAT,,Char,LAT,"Qualifier for anatomical location further detailing laterality of the intervention administration. Examples: ""LEFT"", ""RIGHT"".",26,Interventions,Perm,(LAT),EC,Laterality
Variable Qualifier,EC,ECDIR,,Char,DIR,"Qualifier for anatomical location further detailing directionality. Examples: ""ANTERIOR"", ""LOWER"", ""PROXIMAL"", ""UPPER"".",27,Interventions,Perm,(DIR),EC,Directionality
Variable Qualifier,EC,ECPORTOT,,Char,PORTOT,"Qualifier for anatomical location further detailing distribution, which means arrangement of, apportioning of. Examples: ""ENTIRE"", ""SINGLE"", ""SEGMENT"".",28,Interventions,Perm,(PORTOT),EC,Portion or Totality
Record Qualifier,EC,ECFAST,,Char,FAST,"Indicator used to identify fasting status. Examples: ""Y"", ""N"".",29,Interventions,Perm,(NY),EC,Fasting Status
Record Qualifier,EC,ECPSTRG,,Num,PSTRG,"Amount of an active ingredient expressed quantitatively per dosage unit, per unit of volume, or per unit of weight, according to the pharmaceutical dose form.",30,Interventions,Perm,,EC,Pharmaceutical Strength
Variable Qualifier,EC,ECPSTRGU,,Char,PSTRGU,"Unit for ECPSTRG. Examples: ""mg/TABLET"", ""mg/mL"".",31,Interventions,Perm,,EC,Pharmaceutical Strength Units
Record Qualifier,EC,ECADJ,,Char,ADJ,Describes reason or explanation of why a dose is adjusted.,32,Interventions,Perm,,EC,Reason for Dose Adjustment
Timing,EC,TAETORD,,Num,TAETORD,Number that gives the planned order of the Element within the Arm.,33,Interventions,Perm,,,Planned Order of Element within Arm
Timing,EC,EPOCH,,Char,EPOCH,"Trial Epoch of the exposure as collected record. Examples: ""RUN-IN"", ""TREATMENT"".",34,Interventions,Perm,(EPOCH),,Epoch
Timing,EC,ECSTDTC,,Char,STDTC,The date/time when administration of the treatment indicated by ECTRT and ECDOSE began.,35,Interventions,Exp,ISO 8601,EC,Start Date/Time of Treatment
Timing,EC,ECENDTC,,Char,ENDTC,"The date/time when administration of the treatment indicated by ECTRT and ECDOSE ended. For administrations considered given at a point in time (e.g., oral tablet, pre-filled syringe injection), where only an administration date/time is collected, ECSTDTC should be copied to ECENDTC as the standard representation.",36,Interventions,Exp,ISO 8601,EC,End Date/Time of Treatment
Timing,EC,ECSTDY,,Num,STDY,Study day of ECSTDTC relative to the sponsor-defined DM.RFSTDTC.,37,Interventions,Perm,,EC,Study Day of Start of Treatment
Timing,EC,ECENDY,,Num,ENDY,Study day of ECENDTC relative to the sponsor-defined DM.RFSTDTC.,38,Interventions,Perm,,EC,Study Day of End of Treatment
Timing,EC,ECDUR,,Char,DUR,Collected duration of administration. Used only if collected on the CRF and not derived from start and end date/times.,39,Interventions,Perm,ISO 8601,EC,Duration of Treatment
Timing,EC,ECTPT,,Char,TPT,"Text Description of time when administration should occur. This may be represented as an elapsed time relative to a fixed reference point, such as time of last dose. See ECTPTNUM and ECTPTREF.",40,Interventions,Perm,,EC,Planned Time Point Name
Timing,EC,ECTPTNUM,,Num,TPTNUM,Numerical version of ECTPT to aid in sorting.,41,Interventions,Perm,,EC,Planned Time Point Number
Timing,EC,ECELTM,,Char,ELTM,Planned elapsed time relative to the planned fixed reference (ECTPTREF). This variable is useful where there are repetitive measures. Not a clock time.,42,Interventions,Perm,ISO 8601,EC,Planned Elapsed Time from Time Point Ref
Timing,EC,ECTPTREF,,Char,TPTREF,"Name of the fixed reference point referred to by ECELTM, ECTPTNUM, and ECTPT. Examples: PREVIOUS DOSE, PREVIOUS MEAL.",43,Interventions,Perm,,EC,Time Point Reference
Timing,EC,ECRFTDTC,,Char,RFTDTC,Date/time for a fixed reference time point defined by ECTPTREF.,44,Interventions,Perm,ISO 8601,EC,Date/Time of Reference Time Point
Identifier,EX,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Interventions,Req,,,
Identifier,EX,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Interventions,Req,EX,,
Identifier,EX,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product.,3,Interventions,Req,,,
Identifier,EX,EXSEQ,Sequence Number,Num,SEQ,Sequence Number given to ensure uniqueness of subject records within a domain. May be any valid number.,4,Interventions,Req,,EX,
Identifier,EX,EXGRPID,Group ID,Char,GRPID,Used to tie together a block of related records in a single domain for a subject.,5,Interventions,Perm,,EX,
Identifier,EX,EXREFID,Reference ID,Char,REFID,"Internal or external identifier (e.g., kit number, bottle label, vial identifier).",6,Interventions,Perm,,EX,
Identifier,EX,EXSPID,Sponsor-Defined Identifier,Char,SPID,Sponsor-defined reference number. Perhaps pre-printed on the CRF as an explicit line identifier or defined in the sponsor's operational database. Example: Line number on a CRF Page.,7,Interventions,Perm,,EX,
Identifier,EX,EXLNKID,Link ID,Char,LNKID,Identifier used to link related records across domains.,8,Interventions,Perm,,EX,
Identifier,EX,EXLNKGRP,Link Group ID,Char,LNKGRP,"Identifier used to link related, grouped records across domains.",9,Interventions,Perm,,EX,
Topic,EX,EXTRT,Name of Treatment,Char,TRT,Name of the protocol-specified study treatment given during the dosing period for the observation.,10,Interventions,Req,,EX,
Grouping Qualifier,EX,EXCAT,Category of Treatment,Char,CAT,Used to define a category of EXTRT values.,11,Interventions,Perm,,EX,
Grouping Qualifier,EX,EXSCAT,Subcategory of Treatment,Char,SCAT,A further categorization of EXCAT values.,12,Interventions,Perm,,EX,
Record Qualifier,EX,EXDOSE,Dose,Num,DOSE,Amount of EXTRT when numeric. Not populated when EXDOSTXT is populated.,13,Interventions,Exp,,EX,
Record Qualifier,EX,EXDOSTXT,Dose Description,Char,DOSTXT,Amount of EXTRT when non-numeric. Dosing amounts or a range of dosing information collected in text form. Example: 200-400. Not populated when EXDOSE is populated.,14,Interventions,Perm,,EX,
Variable Qualifier,EX,EXDOSU,Dose Units,Char,DOSU,"Units for EXDOSE, EXDOSTOT, or EXDOSTXT representing protocol-specified values. Examples: "ng", "mg", "mg/kg", "mg/m2".",15,Interventions,Exp,(UNIT),EX,
Variable Qualifier,EX,EXDOSFRM,Dose Form,Char,DOSFRM,"Dose form for EXTRT. Examples: "TABLET", "LOTION".",16,Interventions,Exp,(FRM),EX,
Variable Qualifier,EX,EXDOSFRQ,Dosing Frequency per Interval,Char,DOSFRQ,"Usually expressed as the number of repeated administrations of EXDOSE within a specific time period. Examples: "Q2H", "QD", "BID".",17,Interventions,Perm,(FREQ),EX,
Variable Qualifier,EX,EXDOSRGM,Intended Dose Regimen,Char,DOSRGM,"Text description of the intended schedule or regimen for the Intervention. Example: "TWO WEEKS ON, TWO WEEKS OFF".",18,Interventions,Perm,,EX,
Variable Qualifier,EX,EXROUTE,Route of Administration,Char,ROUTE,"Route of administration for the intervention. Examples: "ORAL", "INTRAVENOUS".",19,Interventions,Perm,(ROUTE),EX,
Record Qualifier,EX,EXLOT,Lot Number,Char,LOT,Lot number of the intervention product.,20,Interventions,Perm,,EX,
Record Qualifier,EX,EXLOC,Location of Dose Administration,Char,LOC,"Specifies location of administration. Examples: "ARM", "LIP".",21,Interventions,Perm,(LOC),EX,
Variable Qualifier,EX,EXLAT,Laterality,Char,LAT,"Qualifier for anatomical location further detailing laterality of the intervention administration. Examples: "LEFT", "RIGHT".",22,Interventions,Perm,(LAT),EX,
Variable Qualifier,EX,EXDIR,Directionality,Char,DIR,"Qualifier for anatomical location further detailing directionality. Examples: "ANTERIOR", "LOWER", "PROXIMAL", "UPPER".",23,Interventions,Perm,(DIR),EX,
Record Qualifier,EX,EXFAST,Fasting Status,Char,FAST,"Indicator used to identify fasting status. Examples: "Y", "N".",24,Interventions,Perm,(NY),EX,
Record Qualifier,EX,EXADJ,Reason for Dose Adjustment,Char,ADJ,Describes reason or explanation of why a dose is adjusted.,25,Interventions,Perm,,EX,
Timing,EX,TAETORD,Planned Order of Element within Arm,Num,TAETORD,Number that gives the planned order of the Element within the Arm.,26,Interventions,Perm,,,
Timing,EX,EPOCH,Epoch,Char,EPOCH,"Trial Epoch of the Exposure record. Examples: "RUN-IN", "TREATMENT".",27,Interventions,Perm,(EPOCH),,
Timing,EX,EXSTDTC,Start Date/Time of Treatment,Char,STDTC,The date/time when administration of the treatment indicated by EXTRT and EXDOSE began.,28,Interventions,Exp,ISO 8601,EX,
Timing,EX,EXENDTC,End Date/Time of Treatment,Char,ENDTC,"The date/time when administration of the treatment indicated by EXTRT and EXDOSE ended. For administrations considered given at a point in time (e.g., oral tablet, pre-filled syringe injection), where only an administration date/time is collected, EXSTDTC should be copied to EXENDTC as the standard representation.",29,Interventions,Exp,ISO 8601,EX,
Timing,EX,EXSTDY,Study Day of Start of Treatment,Num,STDY,Study day of EXSTDTC relative to DM.RFSTDTC.,30,Interventions,Perm,,EX,
Timing,EX,EXENDY,Study Day of End of Treatment,Num,ENDY,Study day of EXENDTC relative to DM.RFSTDTC.,31,Interventions,Perm,,EX,
Timing,EX,EXDUR,Duration of Treatment,Char,DUR,Collected duration of administration. Used only if collected on the CRF and not derived from start and end date/times.,32,Interventions,Perm,ISO 8601,EX,
Timing,EX,EXTPT,Planned Time Point Name,Char,TPT,"1. Text Description of time when administration should occur. \n 2. This may be represented as an elapsed time relative to a fixed reference point, such as time of last dose. See EXTPTNUM and EXTPTREF.",33,Interventions,Perm,,EX,
Timing,EX,EXTPTNUM,Planned Time Point Number,Num,TPTNUM,Numerical version of EXTPT to aid in sorting.,34,Interventions,Perm,,EX,
Timing,EX,EXELTM,Planned Elapsed Time from Time Point Ref,Char,ELTM,Planned elapsed time relative to the planned fixed reference (EXTPTREF). This variable is useful where there are repetitive measures. Not a clock time.,35,Interventions,Perm,ISO 8601,EX,
Timing,EX,EXTPTREF,Time Point Reference,Char,TPTREF,"Name of the fixed reference point referred to by EXELTM, EXTPTNUM, and EXTPT. Examples: PREVIOUS DOSE, PREVIOUS MEAL.",36,Interventions,Perm,,EX,
Timing,EX,EXRFTDTC,Date/Time of Reference Time Point,Char,RFTDTC,Date/time for a fixed reference time point defined by EXTPTREF.,37,Interventions,Perm,ISO 8601,EX,
Identifier,ML,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Interventions,Req,,,
Identifier,ML,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Interventions,Req,ML,,
Identifier,ML,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product.,3,Interventions,Req,,,
Identifier,ML,MLSEQ,Sequence Number,Num,SEQ,Sequence Number given to ensure uniqueness of subject records within a domain. May be any valid number.,4,Interventions,Req,,ML,
Identifier,ML,MLGRPID,Group ID,Char,GRPID,Used to tie together a block of related records in a single domain for a subject.,5,Interventions,Perm,,ML,
Identifier,ML,MLSPID,Sponsor-Defined Identifier,Char,SPID,Sponsor-defined reference number. Examples: a number pre-printed on the CRF as an explicit line identifier or record identifier defined in the sponsor's operational database.,6,Interventions,Perm,,ML,
Topic,ML,MLTRT,Name of Meal,Char,TRT,Verbatim food product name that is either pre-printed or collected on a CRF.,7,Interventions,Req,,ML,
Grouping Qualifier,ML,MLCAT,Category for Meal,Char,CAT,Used to define a category of MLTRT values.,8,Interventions,Perm,,ML,
Grouping Qualifier,ML,MLSCAT,Subcategory for Meal,Char,SCAT,Used to define a further categorization of MLCAT values.,9,Interventions,Perm,,ML,
Variable Qualifier,ML,MLPRESP,ML Pre-specified,Char,PRESP,Used when a specific meal is pre-specified on a CRF. Values should be "Y" or null.,10,Interventions,Perm,(NY),ML,
Record Qualifier,ML,MLOCCUR,ML Occurrence,Char,OCCUR,Used to record whether a pre-specified meal occurred when information about the occurrence of a specific meal is solicited.,11,Interventions,Perm,(NY),ML,
Record Qualifier,ML,MLSTAT,Completion Status,Char,STAT,Used to indicate when a question about the occurrence of a pre-specified meal was not answered. Should be null or have a value of "NOT DONE".,12,Interventions,Perm,(ND),ML,
Record Qualifier,ML,MLREASND,Reason Meal Not Collected,Char,REASND,Describes the reason a response to a question about the occurrence of a meal was not collected. Used in conjunction with MLSTAT when value is "NOT DONE".,13,Interventions,Perm,,ML,
Record Qualifier,ML,MLDOSE,Dose,Num,DOSE,Amount of MLTRT consumed. Not populated when MLDOSTXT is populated.,14,Interventions,Perm,,ML,
Record Qualifier,ML,MLDOSTXT,Dose Description,Char,DOSTXT,"Amount description of MLTRT consumed, collected in text form. Not populated when MLDOSE is populated. Examples: ""<1 per day"", ""200-400"".",15,Interventions,Perm,,ML,
Variable Qualifier,ML,MLDOSU,Dose Units,Char,DOSU,"Units for MLDOSE, MLDOSTOT, or MLDOSTXT.",16,Interventions,Perm,(UNIT),ML,
Variable Qualifier,ML,MLDOSFRM,Dose Form,Char,DOSFRM,"Dosage form for MLTRT. Example: ""BAR, CHEWABLE"".",17,Interventions,Perm,(FRM),ML,
Timing,ML,VISITNUM,Visit Number,Num,VISITNUM,"Clinical encounter number. Numeric version of VISIT, used for sorting.",18,Interventions,Perm,,,
Timing,ML,VISIT,Visit Name,Char,VISIT,Protocol-defined description of a clinical encounter.,19,Interventions,Perm,,,
Timing,ML,VISITDY,Planned Study Day of Visit,Num,VISITDY,Planned study day of VISIT. Should be an integer.,20,Interventions,Perm,,,
Timing,ML,TAETORD,Planned Order of Element within Arm,Num,TAETORD,Number that gives the planned order of the Element within the Arm for the Element in which the meal started.,21,Interventions,Perm,,,
Timing,ML,EPOCH,Epoch,Char,EPOCH,Epoch associated with the start date/time of the meal.,22,Interventions,Perm,(EPOCH),,
Timing,ML,MLDTC,Date/Time of Collection,Char,DTC,Collection date and time of the meal represented in ISO 8601 character format.,23,Interventions,Perm,ISO 8601,ML,
Timing,ML,MLSTDTC,Start Date/Time of Meal,Char,STDTC,Start date/time of the meal represented in ISO 8601 character format.,24,Interventions,Perm,ISO 8601,ML,
Timing,ML,MLENDTC,End Date/Time of Meal,Char,ENDTC,End date/time of the meal represented in ISO 8601 character format.,25,Interventions,Perm,ISO 8601,ML,
Timing,ML,MLDY,Study Day of Visit/Collection/Exam,Num,DY,Actual study day of the visit/collection expressed in integer days relative to the sponsor-defined RFSTDTC in Demographics.,26,Interventions,Perm,,ML,
Timing,ML,MLSTDY,Study Day of Start of Meal,Num,STDY,Actual study day of start of the meal expressed in integer days relative to sponsor-defined RFSTDTC in Demographics.,27,Interventions,Perm,,ML,
Timing,ML,MLENDY,Study Day of End of Meal,Num,ENDY,Actual study day of end of the meal expressed in integer days relative to the sponsor-defined RFSTDTC in Demographics.,28,Interventions,Perm,,ML,
Timing,ML,MLDUR,Duration of Meal,Char,DUR,Collected duration of the meal represented in ISO 8601 character format. Used only if collected on the CRF and not derived.,29,Interventions,Perm,ISO 8601,ML,
Timing,ML,MLTPT,Planned Time Point Name,Char,TPT,Text description of time when a measurement or observation should be taken as defined in the protocol. This may be represented as an elapsed time relative to a fixed reference point. See MLTPTNUM and MLTPTREF.,30,Interventions,Perm,,ML,
Timing,ML,MLTPTNUM,Planned Time Point Number,Num,TPTNUM,Numeric version of planned time point used in sorting.,31,Interventions,Perm,,ML,
Timing,ML,MLELTM,Planned Elapsed Time from Time Point Ref,Char,ELTM,Planned Elapsed time (in ISO 8601) relative to the planned fixed reference (MLTPTREF). This variable is useful when there are repetitive measures. Not a clock time or a date/time variable. Represented as an ISO 8601 duration.,32,Interventions,Perm,ISO 8601,ML,
Timing,ML,MLTPTREF,Time Point Reference,Char,TPTREF,"Description of the fixed reference point referred to by MLELTM, MLTPTNUM, and MLTPT.",33,Interventions,Perm,,ML,
Timing,ML,MLRFTDTC,Date/Time of Reference Time Point,Char,RFTDTC,Date/time for a fixed reference time point defined by MLTPTREF in ISO 8601 character format.,34,Interventions,Perm,ISO 8601,ML,
Timing,ML,MIDS,Disease Milestone Instance Name,Char,MIDS,The name of a specific instance of a Disease Milestone Type (MIDSTYPE) described in the Trial Disease Milestones dataset. This should be unique within a subject. Used only in conjunction with RELMIDS and MIDSDTC.,35,Interventions,Perm,,,
Timing,ML,RELMIDS,Temporal Relation to Milestone Instance,Char,RELMIDS,"The temporal relationship of the observation to the Disease Milestone Instance Name in MIDS. Examples: ""IMMEDIATELY BEFORE"", ""AT TIME OF"", ""AFTER"".",36,Interventions,Perm,,,
Timing,ML,MIDSDTC,Disease Milestone Instance Date/Time,Char,MIDSDTC,"The start date/time of the Disease Milestone Instance Name in MIDS, in ISO 8601 format.",37,Interventions,Perm,ISO 8601,,
Identifier,PR,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Interventions,Req,,,
Identifier,PR,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Interventions,Req,PR,,
Identifier,PR,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product.,3,Interventions,Req,,,
Identifier,PR,PRSEQ,Sequence Number,Num,SEQ,Sequence Number to ensure uniqueness of records within a dataset for a subject. Should be assigned to be in a consistent chronological order.,4,Interventions,Req,,PR,
Identifier,PR,PRGRPID,Group ID,Char,GRPID,Used to link together a block of related records within a subject in a domain.,5,Interventions,Perm,,PR,
Identifier,PR,PRSPID,Sponsor-Defined Identifier,Char,SPID,Sponsor-defined identifier. Example: pre-printed line identifier on a CRF or record identifier defined in the sponsor's operational database.,6,Interventions,Perm,,PR,
Identifier,PR,PRLNKID,Link ID,Char,LNKID,Used to facilitate identification of relationships between records.,7,Interventions,Perm,,PR,
Identifier,PR,PRLNKGRP,Link Group ID,Char,LNKGRP,Used to facilitate identification of relationships between records.,8,Interventions,Perm,,PR,
Topic,PR,PRTRT,Reported Name of Procedure,Char,TRT,"Name of procedure performed, either pre-printed or collected on a CRF.",9,Interventions,Req,,PR,
Synonym Qualifier,PR,PRDECOD,Standardized Procedure Name,Char,DECOD,"Standardized or dictionary-derived name of PRTRT. The sponsor is expected to provide the dictionary name and version used to map the terms in the external codelist element in the Define-XML document. If an intervention term does not have a decode value in the dictionary, then PRDECOD will be null.",10,Interventions,Perm,,PR,
Grouping Qualifier,PR,PRCAT,Category,Char,CAT,Used to define a category of procedure values.,11,Interventions,Perm,,PR,
Grouping Qualifier,PR,PRSCAT,Subcategory,Char,SCAT,Used to define a further categorization of PRCAT values.,12,Interventions,Perm,,PR,
Variable Qualifier,PR,PRPRESP,Pre-specified,Char,PRESP,Used when a specific procedure is pre-specified on a CRF. Values should be "Y" or null.,13,Interventions,Perm,(NY),PR,
Record Qualifier,PR,PROCCUR,Occurrence,Char,OCCUR,Used to record whether a pre-specified procedure occurred when information about the occurrence of a specific procedure is solicited.,14,Interventions,Perm,(NY),PR,
Record Qualifier,PR,PRINDC,Indication,Char,INDC,"Denotes the indication for the procedure (e.g., why the procedure was performed).",15,Interventions,Perm,,PR,
Record Qualifier,PR,PRDOSE,Dose,Num,DOSE,Amount of PRTRT administered. Not populated when PRDOSTXT is populated.,16,Interventions,Perm,,PR,
Record Qualifier,PR,PRDOSTXT,Dose Description,Char,DOSTXT,"Dosing information collected in text form. Examples: ""<1"", ""200-400"". Not populated when PRDOSE is populated.",17,Interventions,Perm,,PR,
Variable Qualifier,PR,PRDOSU,Dose Units,Char,DOSU,"Units for PRDOSE, PRDOSTOT, or PRDOSTXT.",18,Interventions,Perm,(UNIT),PR,
Variable Qualifier,PR,PRDOSFRM,Dose Form,Char,DOSFRM,Dose form for PRTRT.,19,Interventions,Perm,(FRM),PR,
Variable Qualifier,PR,PRDOSFRQ,Dosing Frequency per Interval,Char,DOSFRQ,Usually expressed as the number of doses given per a specific interval.,20,Interventions,Perm,(FREQ),PR,
Variable Qualifier,PR,PRDOSRGM,Intended Dose Regimen,Char,DOSRGM,Text description of the intended schedule or regimen for the procedure.,21,Interventions,Perm,,PR,
Variable Qualifier,PR,PRROUTE,Route of Administration,Char,ROUTE,Route of administration for PRTRT.,22,Interventions,Perm,(ROUTE),PR,
Record Qualifier,PR,PRLOC,Location of Procedure,Char,LOC,Anatomical location of a procedure.,23,Interventions,Perm,(LOC),PR,
Variable Qualifier,PR,PRLAT,Laterality,Char,LAT,Qualifier for anatomical location or specimen further detailing laterality.,24,Interventions,Perm,(LAT),PR,
Variable Qualifier,PR,PRDIR,Directionality,Char,DIR,Qualifier for anatomical location or specimen further detailing directionality.,25,Interventions,Perm,(DIR),PR,
Variable Qualifier,PR,PRPORTOT,Portion or Totality,Char,PORTOT,"Qualifier for anatomical location or specimen further detailing the distribution, which means arrangement of, apportioning of.",26,Interventions,Perm,(PORTOT),PR,
Timing,PR,VISITNUM,Visit Number,Num,VISITNUM,"Clinical encounter number. Numeric version of VISIT, used for sorting.",27,Interventions,Perm,,,
Timing,PR,VISIT,Visit Name,Char,VISIT,Protocol-defined description of a clinical encounter.,28,Interventions,Perm,,,
Timing,PR,VISITDY,Planned Study Day of Visit,Num,VISITDY,Planned study day of VISIT. Should be an integer.,29,Interventions,Perm,,,
Timing,PR,TAETORD,Planned Order of Element within Arm,Num,TAETORD,Number that gives the planned order of the Element within the Arm.,30,Interventions,Perm,,,
Timing,PR,EPOCH,Epoch,Char,EPOCH,Epoch associated with the start date/time of the procedure.,31,Interventions,Perm,(EPOCH),,
Timing,PR,PRSTDTC,Start Date/Time of Procedure,Char,STDTC,Start date/time of the procedure represented in ISO 8601 character format.,32,Interventions,Exp,ISO 8601,PR,
Timing,PR,PRENDTC,End Date/Time of Procedure,Char,ENDTC,End date/time of the procedure represented in ISO 8601 character format.,33,Interventions,Perm,ISO 8601,PR,
Timing,PR,PRSTDY,Study Day of Start of Procedure,Num,STDY,Study day of start of procedure expressed in integer days relative to the sponsor-defined RFSTDTC in Demographics.,34,Interventions,Perm,,PR,
Timing,PR,PRENDY,Study Day of End of Procedure,Num,ENDY,Study day of end of procedure expressed in integer days relative to the sponsor-defined RFSTDTC in Demographics.,35,Interventions,Perm,,PR,
Timing,PR,PRDUR,Duration of Procedure,Char,DUR,Collected duration of a procedure represented in ISO 8601 character format. Used only if collected on the CRF and not derived from start and end date/times.,36,Interventions,Perm,ISO 8601,PR,
Timing,PR,PRTPT,Planned Time Point Name,Char,TPT,"Text description of time when a procedure should be performed. This may be represented as an elapsed time relative to a fixed reference point, such as time of last dose. See PRTPTNUM and PRTPTREF.",37,Interventions,Perm,,PR,
Timing,PR,PRTPTNUM,Planned Time Point Number,Num,TPTNUM,Numerical version of planned time point used in sorting.,38,Interventions,Perm,,PR,
Timing,PR,PRELTM,Planned Elapsed Time from Time Point Ref,Char,ELTM,"Planned elapsed time in ISO 8601 format relative to a planned fixed reference (PRTPTREF). This variable is useful where there are repetitive measures. Not a clock time or a date/time variable, but an interval, represented as ISO duration.",39,Interventions,Perm,ISO 8601,PR,
Timing,PR,PRTPTREF,Time Point Reference,Char,TPTREF,"Description of the fixed reference point referred to by PRELTM, PRTPTNUM, and PRTPT.",40,Interventions,Perm,,PR,
Timing,PR,PRRFTDTC,Date/Time of Reference Time Point,Char,RFTDTC,Date/time for a fixed reference time point defined by PRTRTREF in ISO 8601 character format.,41,Interventions,Perm,ISO 8601,PR,
Timing,PR,PRSTRTPT,Start Relative to Reference Time Point,Char,STRTPT,"Identifies the start of the observation as being before or after the sponsor-defined reference time point defined by variable PRSTTPT. \n Not all values of the codelist are allowable for this variable. See Section 4.4.7, Use of Relative Timing Variables.",42,Interventions,Perm,(STENRF),PR,
Timing,PR,PRSTTPT,Start Reference Time Point,Char,STTPT,Description or date/time in ISO 8601 character format of the sponsor-defined reference point referred to by PRSTRTPT. Examples: "2003-12-15" or "VISIT 1".,43,Interventions,Perm,,PR,
Timing,PR,PRENRTPT,End Relative to Reference Time Point,Char,ENRTPT,"Identifies the end of the observation as being before or after the sponsor-defined reference time point defined by variable PRENTPT. \n Not all values of the codelist are allowable for this variable. See Section 4.4.7, Use of Relative Timing Variables.",44,Interventions,Perm,(STENRF),PR,
Timing,PR,PRENTPT,End Reference Time Point,Char,ENTPT,Description or date/time in ISO 8601 character format of the sponsor-defined reference point referred to by PRENRTPT. Examples: "2003-12-25" or "VISIT 2".,45,Interventions,Perm,,PR,
Identifier,SU,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Interventions,Req,,,
Identifier,SU,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Interventions,Req,SU,,
Identifier,SU,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product.,3,Interventions,Req,,,
Identifier,SU,SUSEQ,Sequence Number,Num,SEQ,Sequence Number given to ensure uniqueness of subject records within a domain. May be any valid number.,4,Interventions,Req,,SU,
Identifier,SU,SUGRPID,Group ID,Char,GRPID,Used to tie together a block of related records in a single domain for a subject.,5,Interventions,Perm,,SU,
Identifier,SU,SUSPID,Sponsor-Defined Identifier,Char,SPID,Sponsor-defined reference number. Perhaps pre-printed on the CRF as an explicit line identifier or defined in the sponsor's operational database. Example: Line number on a Tobacco & Alcohol use CRF page.,6,Interventions,Perm,,SU,
Topic,SU,SUTRT,Reported Name of Substance,Char,TRT,"Substance name. Examples: ""Cigarettes"", ""Coffee"".",7,Interventions,Req,,SU,
Synonym Qualifier,SU,SUMODIFY,Modified Substance Name,Char,MODIFY,"If SUTRT is modified, then the modified text is placed here.",8,Interventions,Perm,,SU,
Synonym Qualifier,SU,SUDECOD,Standardized Substance Name,Char,DECOD,Standardized or dictionary-derived text description of SUTRT or SUMODIFY if the sponsor chooses to code the substance use. The sponsor is expected to provide the dictionary name and version used to map the terms utilizing the external codelist element in the Define-XML document.,9,Interventions,Perm,,SU,
Grouping Qualifier,SU,SUCAT,Category for Substance Use,Char,CAT,"Used to define a category of related records. Examples: ""TOBACCO"", ""ALCOHOL"", or ""CAFFEINE"".",10,Interventions,Perm,,SU,
Grouping Qualifier,SU,SUSCAT,Subcategory for Substance Use,Char,SCAT,"A further categorization of substance use. Examples: ""CIGARS"", ""CIGARETTES"", ""BEER"", ""WINE"".",11,Interventions,Perm,,SU,
Variable Qualifier,SU,SUPRESP,SU Pre-Specified,Char,PRESP,Used to indicate whether ("Y"/null) information about the use of a specific substance was solicited on the CRF.,12,Interventions,Perm,(NY),SU,
Record Qualifier,SU,SUOCCUR,SU Occurrence,Char,OCCUR,"When the use of specific substances is solicited, SUOCCUR is used to indicate whether or not (""Y""/""N"") a particular pre-specified substance was used. Values are null for substances not specifically solicited.",13,Interventions,Perm,(NY),SU,
Record Qualifier,SU,SUSTAT,Completion Status,Char,STAT,"When the use of pre-specified substances is solicited, the completion status indicates that there was no response to the question about the pre-specified substance. When there is no pre-specified list on the CRF, then the completion status indicates that substance use was not assessed for the subject.",14,Interventions,Perm,(ND),SU,
Record Qualifier,SU,SUREASND,Reason Substance Use Not Collected,Char,REASND,Describes the reason substance use was not collected. Used in conjunction with SUSTAT when value of SUSTAT is "NOT DONE".,15,Interventions,Perm,,SU,
Variable Qualifier,SU,SUCLAS,Substance Use Class,Char,CLAS,"Substance use class. May be obtained from coding. When coding to a single class, populate with class value. If using a dictionary and coding to multiple classes, then follow Section 4.2.8.3, Multiple Values for a Non-Result Qualifier Variable, or omit SUCLAS.",16,Interventions,Perm,,SU,
Variable Qualifier,SU,SUCLASCD,Substance Use Class Code,Char,CLASCD,Code corresponding to SUCLAS. May be obtained from coding.,17,Interventions,Perm,,SU,
Record Qualifier,SU,SUDOSE,Substance Use Consumption,Num,DOSE,Amount of SUTRT consumed. Not populated if SUDOSTXT is populated.,18,Interventions,Perm,,SU,
Record Qualifier,SU,SUDOSTXT,Substance Use Consumption Text,Char,DOSTXT,Substance use consumption amounts or a range of consumption information collected in text form. Not populated if SUDOSE is populated.,19,Interventions,Perm,,SU,
Variable Qualifier,SU,SUDOSU,Consumption Units,Char,DOSU,"Units for SUDOSE, SUDOSTOT, or SUDOSTXT. Examples: ""OUNCES"", ""CIGARETTE EQUIVALENTS"", ""GRAMS"".",20,Interventions,Perm,(UNIT),SU,
Variable Qualifier,SU,SUDOSFRM,Dose Form,Char,DOSFRM,"Dose form for SUTRT. Examples: ""INJECTABLE"", ""LIQUID"", or ""POWDER"".",21,Interventions,Perm,,SU,
Variable Qualifier,SU,SUDOSFRQ,Use Frequency Per Interval,Char,DOSFRQ,Usually expressed as the number of repeated administrations of SUDOSE within a specific time period. Example: "Q24H" (every day).,22,Interventions,Perm,(FREQ),SU,
Record Qualifier,SU,SUDOSTOT,Total Daily Consumption,Num,DOSTOT,"Total daily use of SUTRT using the units in SUDOSU. Used when dosing is collected as Total Daily Dose. If sponsor needs to aggregate the data over a period other than daily, then the aggregated total could be recorded in a Supplemental Qualifier variable.",23,Interventions,Perm,,SU,
Variable Qualifier,SU,SUROUTE,Route of Administration,Char,ROUTE,"Route of administration for SUTRT. Examples: ""ORAL"", ""INTRAVENOUS"".",24,Interventions,Perm,(ROUTE),SU,
Timing,SU,TAETORD,Planned Order of Element within Arm,Num,TAETORD,Number that gives the planned order of the Element within the Arm for the Element in which the substance use started. Null for substances that started before study participation.,25,Interventions,Perm,,,
Timing,SU,EPOCH,Epoch,Char,EPOCH,Epoch associated with the start date/time of the substance use. Null for substances that started before study participation.,26,Interventions,Perm,(EPOCH),,
Timing,SU,SUSTDTC,Start Date/Time of Substance Use,Char,STDTC,Start date/time of the substance use represented in ISO 8601 character format.,27,Interventions,Perm,ISO 8601,SU,
Timing,SU,SUENDTC,End Date/Time of Substance Use,Char,ENDTC,End date/time of the substance use represented in ISO 8601 character format.,28,Interventions,Perm,ISO 8601,SU,
Timing,SU,SUSTDY,Study Day of Start of Substance Use,Num,STDY,Study day of start of substance use relative to the sponsor-defined RFSTDTC.,29,Interventions,Perm,,SU,
Timing,SU,SUENDY,Study Day of End of Substance Use,Num,ENDY,Study day of end of substance use relative to the sponsor-defined RFSTDTC.,30,Interventions,Perm,,SU,
Timing,SU,SUDUR,Duration of Substance Use,Char,DUR,Collected duration of substance use in ISO 8601 format. Used only if collected on the CRF and not derived from start and end date/times.,31,Interventions,Perm,ISO 8601,SU,
Timing,SU,SUSTRF,Start Relative to Reference Period,Char,STRF,"Describes the start of the substance use relative to the sponsor-defined reference period. The sponsor-defined reference period is a continuous period of time defined by a discrete starting point and a discrete ending point (represented by RFSTDTC and RFENDTC in Demographics). If information such as ""PRIOR"" was collected, this information may be translated into SUSTRF. \n Not all values of the codelist are allowable for this variable. See Section 4.4.7, Use of Relative Timing Variables.",32,Interventions,Perm,(STENRF),SU,
Timing,SU,SUENRF,End Relative to Reference Period,Char,ENRF,"Describes the end of the substance use with relative to the sponsor-defined reference period. The sponsor-defined reference period is a continuous period of time defined by a discrete starting point and a discrete ending point (represented by RFSTDTC and RFENDTC in Demographics). If information such as ""PRIOR"", ""ONGOING"", or ""CONTINUING"" was collected, this information may be translated into SUENRF. \n Not all values of the codelist are allowable for this variable. See Section 4.4.7, Use of Relative Timing Variables.",33,Interventions,Perm,(STENRF),SU,
Timing,SU,SUSTRTPT,Start Relative to Reference Time Point,Char,STRTPT,"Identifies the start of the substance as being before or after the reference time point defined by variable SUSTTPT. \n Not all values of the codelist are allowable for this variable. See Section 4.4.7 , Use of Relative Timing Variables.",34,Interventions,Perm,(STENRF),SU,
Timing,SU,SUSTTPT,Start Reference Time Point,Char,STTPT,Description or date/time in ISO 8601 character format of the reference point referred to by SUSTRTPT. Examples: "2003-12-15" or "VISIT 1".,35,Interventions,Perm,,SU,
Timing,SU,SUENRTPT,End Relative to Reference Time Point,Char,ENRTPT,"Identifies the end of the substance as being before or after the reference time point defined by variable SUENTPT. \n Not all values of the codelist are allowable for this variable. See Section 4.4.7 , Use of Relative Timing Variables.",36,Interventions,Perm,(STENRF),SU,
Timing,SU,SUENTPT,End Reference Time Point,Char,ENTPT,Description or date/time in ISO 8601 character format of the reference point referred to by SUENRTPT. Examples: "2003-12-25" or "VISIT 2".,37,Interventions,Perm,,SU,
Identifier,AE,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Events,Req,,,
Identifier,AE,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Events,Req,AE,,
Identifier,AE,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product.,3,Events,Req,,,
Identifier,AE,AESEQ,Sequence Number,Num,SEQ,Sequence number given to ensure uniqueness of subject records within a domain. May be any valid number.,4,Events,Req,,AE,
Identifier,AE,AEGRPID,Group ID,Char,GRPID,Used to tie together a block of related records in a single domain for a subject.,5,Events,Perm,,AE,
Identifier,AE,AEREFID,Reference ID,Char,REFID,Internal or external identifier such as a serial number on an SAE reporting form.,6,Events,Perm,,AE,
Identifier,AE,AESPID,Sponsor-Defined Identifier,Char,SPID,Sponsor-defined identifier. It may be preprinted on the CRF as an explicit line identifier or defined in the sponsor's operational database. Example: Line number on an Adverse Events page.,7,Events,Perm,,AE,
Topic,AE,AETERM,Reported Term for the Adverse Event,Char,TERM,Verbatim name of the event.,8,Events,Req,,AE,
Synonym Qualifier,AE,AEMODIFY,Modified Reported Term,Char,MODIFY,"If AETERM is modified to facilitate coding, then AEMODIFY will contain the modified text.",9,Events,Perm,,AE,
Variable Qualifier,AE,AELLT,Lowest Level Term,Char,LLT,Dictionary-derived text description of the Lowest Level Term.,10,Events,Exp,MedDRA,AE,
Variable Qualifier,AE,AELLTCD,Lowest Level Term Code,Num,LLTCD,Dictionary-derived code for the Lowest Level Term.,11,Events,Exp,MedDRA,AE,
Synonym Qualifier,AE,AEDECOD,Dictionary-Derived Term,Char,DECOD,Dictionary-derived text description of AETERM or AEMODIFY. Equivalent to the Preferred Term (PT in MedDRA). The sponsor is expected to provide the dictionary name and version used to map the terms utilizing the external codelist element in the Define-XML document.,12,Events,Req,MedDRA,AE,
Variable Qualifier,AE,AEPTCD,Preferred Term Code,Num,PTCD,Dictionary-derived code for the Preferred Term.,13,Events,Exp,MedDRA,AE,
Variable Qualifier,AE,AEHLT,High Level Term,Char,HLT,Dictionary-derived text description of the High Level Term for the primary System Organ Class.,14,Events,Exp,MedDRA,AE,
Variable Qualifier,AE,AEHLTCD,High Level Term Code,Num,HLTCD,Dictionary-derived code for the High Level Term for the primary System Organ Class.,15,Events,Exp,MedDRA,AE,
Variable Qualifier,AE,AEHLGT,High Level Group Term,Char,HLGT,Dictionary-derived text description of the High Level Group Term for the primary System Organ Class.,16,Events,Exp,MedDRA,AE,
Variable Qualifier,AE,AEHLGTCD,High Level Group Term Code,Num,HLGTCD,Dictionary-derived code for the High Level Group Term for the primary System Organ Class.,17,Events,Exp,MedDRA,AE,
Grouping Qualifier,AE,AECAT,Category for Adverse Event,Char,CAT,"Used to define a category of related records. Example: ""BLEEDING"", ""NEUROPSYCHIATRIC"".",18,Events,Perm,,AE,
Grouping Qualifier,AE,AESCAT,Subcategory for Adverse Event,Char,SCAT,A further categorization of adverse event. Example: "NEUROLOGIC".,19,Events,Perm,,AE,
Variable Qualifier,AE,AEPRESP,Pre-Specified Adverse Event,Char,PRESP,"A value of ""Y"" indicates that this adverse event was pre-specified on the CRF. Values are null for spontaneously reported events (i.e., those collected as free-text verbatim terms).",20,Events,Perm,(NY),AE,
Record Qualifier,AE,AEBODSYS,Body System or Organ Class,Char,BODSYS,"Dictionary derived. Body system or organ class used by the sponsor from the coding dictionary (e.g., MedDRA). When using a multi-axial dictionary such as MedDRA, this should contain the SOC used for the sponsor's analyses and summary tables, which may not necessarily be the primary SOC.",21,Events,Exp,,AE,
Variable Qualifier,AE,AEBDSYCD,Body System or Organ Class Code,Num,BDSYCD,"Dictionary derived. Code for the body system or organ class used by the sponsor. When using a multi-axial dictionary such as MedDRA, this should contain the SOC used for the sponsor's analyses and summary tables, which may not necessarily be the primary SOC.",22,Events,Exp,MedDRA,AE,
Variable Qualifier,AE,AESOC,Primary System Organ Class,Char,SOC,Dictionary-derived text description of the primary System Organ Class. Will be the same as AEBODSYS if the primary SOC was used for analysis.,23,Events,Exp,MedDRA,AE,
Variable Qualifier,AE,AESOCCD,Primary System Organ Class Code,Num,SOCCD,Dictionary-derived code for the primary System Organ Class. Will be the same as AEBDSYCD if the primary SOC was used for analysis.,24,Events,Exp,MedDRA,AE,
Record Qualifier,AE,AELOC,Location of Event,Char,LOC,"Describes anatomical location relevant for the event (e.g., ""ARM"" for skin rash).",25,Events,Perm,(LOC),AE,
Record Qualifier,AE,AESEV,Severity/Intensity,Char,SEV,"The severity or intensity of the event. Examples: ""MILD"", ""MODERATE"", ""SEVERE"".",26,Events,Perm,(AESEV),AE,
Record Qualifier,AE,AESER,Serious Event,Char,SER,Is this a serious event? Valid values are "Y" and "N".,27,Events,Exp,(NY),AE,
Record Qualifier,AE,AEACN,Action Taken with Study Treatment,Char,ACN,"Describes changes to the study treatment as a result of the event. AEACN is specifically for the relationship to study treatment. AEACNOTH is for actions unrelated to dose adjustments of study treatment. Examples of AEACN values include ICH E2B values: ""DRUG WITHDRAWN"", ""DOSE REDUCED"", ""DOSE INCREASED"", ""DOSE NOT CHANGED"", ""UNKNOWN"" or ""NOT APPLICABLE"".",28,Events,Exp,(ACN),AE,
Record Qualifier,AE,AEACNOTH,Other Action Taken,Char,ACNOTH,Describes other actions taken as a result of the event that are unrelated to dose adjustments of study treatment. Usually reported as free text. Example: "TREATMENT UNBLINDED. PRIMARY CARE PHYSICIAN NOTIFIED".,29,Events,Perm,,AE,
Record Qualifier,AE,AEREL,Causality,Char,REL,"Records the investigator's opinion as to the causality of the event to the treatment. ICH E2A and E2B examples include ""NOT RELATED"", ""UNLIKELY RELATED"", ""POSSIBLY RELATED"", ""RELATED"". Controlled Terminology may be defined in the future. Check with regulatory authority for population of this variable.",30,Events,Exp,,AE,
Record Qualifier,AE,AERELNST,Relationship to Non-Study Treatment,Char,RELNST,Records the investigator's opinion as to whether the event may have been due to a treatment other than study drug. May be reported as free text. Example: "MORE LIKELY RELATED TO ASPIRIN USE".,31,Events,Perm,,AE,
Record Qualifier,AE,AEPATT,Pattern of Adverse Event,Char,PATT,"Used to indicate the pattern of the event over time. Examples: ""INTERMITTENT"", ""CONTINUOUS"", ""SINGLE EVENT"".",32,Events,Perm,,AE,
Record Qualifier,AE,AEOUT,Outcome of Adverse Event,Char,OUT,Description of the outcome of an event.,33,Events,Perm,(OUT),AE,
Record Qualifier,AE,AESCAN,Involves Cancer,Char,SCAN,Was the serious event associated with the development of cancer? Valid values are "Y" and "N". This is a legacy seriousness criterion. It is not included in ICH E2A.,34,Events,Perm,(NY),AE,
Record Qualifier,AE,AESCONG,Congenital Anomaly or Birth Defect,Char,SCONG,Was the serious event associated with congenital anomaly or birth defect? Valid values are "Y" and "N".,35,Events,Perm,(NY),AE,
Record Qualifier,AE,AESDISAB,Persist or Signif Disability/Incapacity,Char,SDISAB,Did the serious event result in persistent or significant disability/incapacity? Valid values are "Y" and "N".,36,Events,Perm,(NY),AE,
Record Qualifier,AE,AESDTH,Results in Death,Char,SDTH,Did the serious event result in death? Valid values are "Y" and "N".,37,Events,Perm,(NY),AE,
Record Qualifier,AE,AESHOSP,Requires or Prolongs Hospitalization,Char,SHOSP,Did the serious event require or prolong hospitalization? Valid values are "Y" and "N".,38,Events,Perm,(NY),AE,
Record Qualifier,AE,AESLIFE,Is Life Threatening,Char,SLIFE,Was the serious event life threatening? Valid values are "Y" and "N".,39,Events,Perm,(NY),AE,
Record Qualifier,AE,AESOD,Occurred with Overdose,Char,SOD,Did the serious event occur with an overdose? Valid values are "Y" and "N". This is a legacy seriousness criterion. It is not included in ICH E2A.,40,Events,Perm,(NY),AE,
Record Qualifier,AE,AESMIE,Other Medically Important Serious Event,Char,SMIE,Do additional categories for seriousness apply? Valid values are "Y" and "N".,41,Events,Perm,(NY),AE,
Record Qualifier,AE,AECONTRT,Concomitant or Additional Trtmnt Given,Char,CONTRT,Was another treatment given because of the occurrence of the event? Valid values are "Y" and "N".,42,Events,Perm,(NY),AE,
Record Qualifier,AE,AETOXGR,Standard Toxicity Grade,Char,TOXGR,"Toxicity grade according to a standard toxicity scale such as Common Terminology Criteria for Adverse Events v3.0 (CTCAE). Sponsor should specify name of the scale and version used in the metadata (see Assumption 6d). If value is from a numeric scale, represent only the number (e.g., ""2"" and not ""Grade 2"").",43,Events,Perm,,AE,
Timing,AE,TAETORD,Planned Order of Element within Arm,Num,TAETORD,Number that gives the planned order of the Element within the Arm.,44,Events,Perm,,,
Timing,AE,EPOCH,Epoch,Char,EPOCH,"Epoch associated with the start date/time of the adverse event. Examples: ""SCREENING"", ""TREATMENT"", ""FOLLOW-UP"".",45,Events,Perm,(EPOCH),,
Timing,AE,AESTDTC,Start Date/Time of Adverse Event,Char,STDTC,Start date/time of the adverse event represented in ISO 8601 character format.,46,Events,Exp,ISO 8601,AE,
Timing,AE,AEENDTC,End Date/Time of Adverse Event,Char,ENDTC,End date/time of the adverse event represented in ISO 8601 character format.,47,Events,Exp,ISO 8601,AE,
Timing,AE,AESTDY,Study Day of Start of Adverse Event,Num,STDY,Study day of start of adverse event relative to the sponsor-defined RFSTDTC.,48,Events,Perm,,AE,
Timing,AE,AEENDY,Study Day of End of Adverse Event,Num,ENDY,Study day of end of event relative to the sponsor-defined RFSTDTC.,49,Events,Perm,,AE,
Timing,AE,AEDUR,Duration of Adverse Event,Char,DUR,"Collected duration and unit of an adverse event. Used only if collected on the CRF and not derived from start and end date/times. Example: ""P1DT2H"" (for 1 day, 2 hours).",50,Events,Perm,ISO 8601,AE,
Timing,AE,AEENRF,End Relative to Reference Period,Char,ENRF,"Describes the end of the event relative to the sponsor-defined reference period. The sponsor-defined reference period is a continuous period of time defined by a discrete starting point (RFSTDTC) and a discrete ending point (RFENDTC) of the trial. \n Not all values of the codelist are allowable for this variable. See Section 4.4.7, Use of Relative Timing Variables.",51,Events,Perm,(STENRF),AE,
Timing,AE,AEENRTPT,End Relative to Reference Time Point,Char,ENRTPT,"Identifies the end of the event as being before or after the reference time point defined by variable AEENTPT. \n Not all values of the codelist are allowable for this variable. See Section 4.4.7, Use of Relative Timing Variables.",52,Events,Perm,(STENRF),AE,
Timing,AE,AEENTPT,End Reference Time Point,Char,ENTPT,Description of date/time in ISO 8601 character format of the reference point referred to by AEENRTPT. Examples: "2003-12-25" or "VISIT 2".,53,Events,Perm,,AE,
Identifier,CE,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Events,Req,,,
Identifier,CE,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Events,Req,CE,,
Identifier,CE,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product.,3,Events,Req,,,
Identifier,CE,CESEQ,Sequence Number,Num,SEQ,Sequence Number given to ensure uniqueness of subject records within adomain. May be any valid number.,4,Events,Req,,CE,
Identifier,CE,CEGRPID,Group ID,Char,GRPID,Used to link together a block of related records for a subject within a domain.,5,Events,Perm,,CE,
Identifier,CE,CEREFID,Reference ID,Char,REFID,"Internal or external identifier such as lab specimen ID, or UUID for an ECG waveform or a medical image.",6,Events,Perm,,CE,
Identifier,CE,CESPID,Sponsor-Defined Identifier,Char,SPID,Sponsor-defined identifier.,7,Events,Perm,,CE,
Topic,CE,CETERM,Reported Term for the Clinical Event,Char,TERM,Term for the medical condition or event. Most likely preprinted on CRF.,8,Events,Req,,CE,
Synonym Qualifier,CE,CEDECOD,Dictionary-Derived Term,Char,DECOD,Controlled terminology for the name of the clinical event. The sponsor is expected to provide the dictionary name and version used to map the terms utilizing the external codelist element in the Define-XML document.,9,Events,Perm,,CE,
Grouping Qualifier,CE,CECAT,Category for the Clinical Event,Char,CAT,Used to define a category of related records.,10,Events,Perm,,CE,
Grouping Qualifier,CE,CESCAT,Subcategory for the Clinical Event,Char,SCAT,A further categorization of the condition or event.,11,Events,Perm,,CE,
Variable Qualifier,CE,CEPRESP,Clinical Event Pre-specified,Char,PRESP,Used to indicate whether the Event in CETERM was pre-specified. Value is &quot;Y&quot; for pre-specified events and null for spontaneously reported events.,12,Events,Perm,(NY),CE,
Record Qualifier,CE,CEOCCUR,Clinical Event Occurrence,Char,OCCUR,"Used when the occurrence of specific events is solicited, to indicate whether or not a clinical event occurred. Values are null for spontaneously reported events.",13,Events,Perm,(NY),CE,
Record Qualifier,CE,CESTAT,Completion Status,Char,STAT,The status indicates that a question from a pre-specified list was not answered.,14,Events,Perm,(ND),CE,
Record Qualifier,CE,CEREASND,Reason Clinical Event Not Collected,Char,REASND,Describes the reason clinical event data was not collected. Used in conjunction with CESTAT when value is &quot;NOT DONE&quot;.,15,Events,Perm,,CE,
Record Qualifier,CE,CEBODSYS,Body System or Organ Class,Char,BODSYS,"Dictionary-derived. Body system or organ class that is involved in an event or measurement from a standard hierarchy (e.g., MedDRA). When using a multiaxial dictionary such as MedDRA, this should contain the SOC used for the sponsor's analyses and summary tables which may not necessarily be the primary SOC.",16,Events,Perm,,CE,
Record Qualifier,CE,CESEV,Severity/Intensity,Char,SEV,"The severity or intensity of the event. Examples: &quot;MILD&quot;, &quot;MODERATE&quot;, &quot;SEVERE&quot;.",17,Events,Perm,,CE,
Timing,CE,TAETORD,Planned Order of Element within Arm,Num,TAETORD,Number that gives the planned order of the Element within the Arm for the Element in which the clinical event started.,18,Events,Perm,,,
Timing,CE,EPOCH,Epoch,Char,EPOCH,Epoch associated with the start date/time of the clinical event.,19,Events,Perm,(EPOCH),,
Timing,CE,CEDTC,Date/Time of Event Collection,Char,DTC,Collection date and time for the clinical event observation represented in ISO 8601 character format.,20,Events,Perm,ISO 8601,CE,
Timing,CE,CESTDTC,Start Date/Time of Clinical Event,Char,STDTC,Start date/time of the clinical event represented in ISO 8601 character format.,21,Events,Perm,ISO 8601,CE,
Timing,CE,CEENDTC,End Date/Time of Clinical Event,Char,ENDTC,"End date/time of the clinical event, represented in ISO 8601 character format.",22,Events,Perm,ISO 8601,CE,
Timing,CE,CEDY,Study Day of Event Collection,Num,DY,"1. Study day of clinical event collection, measured as integer days. \n 2. Algorithm for calculations must be relative to the sponsor-defined RFSTDTC variable in Demographics. This formula should be consistent across the submission.",23,Events,Perm,,CE,
Timing,CE,CESTDY,Study Day of Start of Event,Num,STDY,Actual study day of start of the clinical event expressed in integer days relative to the sponsor-defined RFSTDTC in Demographics.,24,Events,Perm,,CE,
Timing,CE,CEENDY,Study Day of End of Event,Num,ENDY,Actual study day of end of the clinical event expressed in integer days relative to the sponsor-defined RFSTDTC in Demographics.,25,Events,Perm,,CE,
Timing,CE,CESTRF,Start Relative to Reference Period,Char,STRF,"Describes the start of the clinical event relative to the sponsor-defined reference period. The sponsor-defined reference period is a continuous period of time defined by a discrete starting point and a discrete ending point (represented by RFSTDTC and RFENDTC in Demographics). \n Not all values of the codelist are allowable for this variable. See Section 4.4.7, Use of Relative Timing Variables.",26,Events,Perm,(STENRF),CE,
Timing,CE,CEENRF,End Relative to Reference Period,Char,ENRF,"Describes the end of the event relative to the sponsor-defined reference period. The sponsor-defined reference period is a continuous period of time defined by a discrete starting point and a discrete ending point (represented by RFSTDTC and RFENDTC in Demographics). \n Not all values of the codelist are allowable for this variable. See Section 4.4.7, Use of Relative Timing Variables.",27,Events,Perm,(STENRF),CE,
Timing,CE,CESTRTPT,Start Relative to Reference Time Point,Char,STRTPT,"Identifies the start of the observation as being before or after the reference time point defined by variable CESTTPT. \n Not all values of the codelist are allowable for this variable. See Section 4.4.7, Use of Relative Timing Variables.",28,Events,Perm,(STENRF),CE,
Timing,CE,CESTTPT,Start Reference Time Point,Char,STTPT,Description or date/time in ISO 8601 character format of the sponsor-defined reference point referred to by --STRTPT. Examples: &quot;2003-12-15&quot; or &quot;VISIT 1&quot;.,29,Events,Perm,,CE,
Timing,CE,CEENRTPT,End Relative to Reference Time Point,Char,ENRTPT,"Identifies the end of the observation as being before or after the sponsor-defined reference time point defined by variable CEENTPT. \n Not all values of the codelist are allowable for this variable. See Section 4.4.7, Use of Relative Timing Variables.",30,Events,Perm,(STENRF),CE,
Timing,CE,CEENTPT,End Reference Time Point,Char,ENTPT,Description or date/time in ISO 8601 character format of the reference point referred to by CEENRTPT. Examples: &quot;2003-12-25&quot; or &quot;VISIT 2&quot;.,31,Events,Perm,,CE,
Identifier,DS,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Events,Req,,,
Identifier,DS,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Events,Req,DS,,
Identifier,DS,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product.,3,Events,Req,,,
Identifier,DS,DSSEQ,Sequence Number,Num,SEQ,Sequence Number given to ensure uniqueness of subject records within a domain. May be any valid number.,4,Events,Req,,DS,
Identifier,DS,DSGRPID,Group ID,Char,GRPID,Used to tie together a block of related records in a single domain for a subject.,5,Events,Perm,,DS,
Identifier,DS,DSREFID,Reference ID,Char,REFID,Internal or external identifier.,6,Events,Perm,,DS,
Identifier,DS,DSSPID,Sponsor-Defined Identifier,Char,SPID,Sponsor-defined reference number. Perhaps preprinted on the CRF as an explicit line identifier or defined in the sponsor's operational database. Example: Line number on a Disposition page.,7,Events,Perm,,DS,
Topic,DS,DSTERM,Reported Term for the Disposition Event,Char,TERM,"Verbatim name of the event or protocol milestone. Some terms in DSTERM will match DSDECOD, but others, such as ""Subject moved"" will map to controlled terminology in DSDECOD, such as ""LOST TO FOLLOW-UP"".",8,Events,Req,,DS,
Synonym Qualifier,DS,DSDECOD,Standardized Disposition Term,Char,DECOD,"Controlled terminology for the name of disposition event or protocol milestone. Examples of protocol milestones: ""INFORMED CONSENT OBTAINED"", ""RANDOMIZED"". There are separate codelists used for DSDECOD where the choice depends on the value of DSCAT. Codelist ""NCOMPLT"" is used for disposition events and codelist ""PROTMLST"" is used for protocol milestones. The variable may be subject to controlled terminology for other events.",9,Events,Req,(NCOMPLT)(PROTMLST),DS,
Grouping Qualifier,DS,DSCAT,Category for Disposition Event,Char,CAT,Used to define a category of related records.,10,Events,Exp,(DSCAT),DS,
Grouping Qualifier,DS,DSSCAT,Subcategory for Disposition Event,Char,SCAT,"A further categorization of DSCAT (e.g., ""STUDY PARTICIPATION"", ""STUDY TREATMENT"" when DSCAT = ""DISPOSITION EVENT"").",11,Events,Perm,,DS,
Timing,DS,EPOCH,Epoch,Char,EPOCH,Epoch associated with the start date/time of the event.,12,Events,Perm,(EPOCH),,
Timing,DS,DSDTC,Date/Time of Collection,Char,DTC,Collection date and time of the disposition observation represented in ISO 8601 character format.,13,Events,Perm,ISO 8601,DS,
Timing,DS,DSSTDTC,Start Date/Time of Disposition Event,Char,STDTC,Start date/time of the disposition event in ISO 8601 character format.,14,Events,Exp,ISO 8601,DS,
Timing,DS,DSDY,Study Day of Collection,Num,DY,Start date/time of the disposition event in ISO 8601 character format.,15,Events,Exp,,DS,
Timing,DS,DSSTDY,Study Day of Start of Disposition Event,Num,STDY,Study day of start of event relative to the sponsor-defined RFSTDTC.,16,Events,Perm,,DS,
Identifier,DV,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Events,Req,,,
Identifier,DV,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Events,Req,DV,,
Identifier,DV,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product.,3,Events,Req,,,
Identifier,DV,DVSEQ,Sequence Number,Num,SEQ,Sequence Number given to ensure uniqueness of subject records within a domain. May be any valid number.,4,Events,Req,,DV,
Identifier,DV,DVREFID,Reference ID,Char,REFID,Internal or external identifier.,5,Events,Perm,,DV,
Identifier,DV,DVSPID,Sponsor-Defined Identifier,Char,SPID,Sponsor-defined reference number. Perhaps preprinted on the CRF as an explicit line identifier or defined in the sponsor's operational database. Example: Line number on a CRF page.,6,Events,Perm,,DV,
Topic,DV,DVTERM,Protocol Deviation Term,Char,TERM,"Verbatim name of the protocol deviation criterion. Example: ""IVRS PROCESS DEVIATION - NO DOSE CALL PERFORMED"". The DVTERM values will map to the controlled terminology in DVDECOD, such as ""TREATMENT DEVIATION"".",7,Events,Req,,DV,
Synonym Qualifier,DV,DVDECOD,Protocol Deviation Coded Term,Char,DECOD,"Controlled terminology for the name of the protocol deviation. Examples: ""SUBJECT NOT WITHDRAWN AS PER PROTOCOL"", ""SELECTION CRITERIA NOT MET"", ""EXCLUDED CONCOMITANT MEDICATION"", ""TREATMENT DEVIATION"".",8,Events,Perm,,DV,
Grouping Qualifier,DV,DVCAT,Category for Protocol Deviation,Char,CAT,Category of the protocol deviation criterion.,9,Events,Perm,,DV,
Grouping Qualifier,DV,DVSCAT,Subcategory for Protocol Deviation,Char,SCAT,A further categorization of the protocol deviation.,10,Events,Perm,,DV,
Timing,DV,TAETORD,Planned Order of Element within Arm,Num,TAETORD,Number that gives the planned order of the Element within the Arm.,11,Events,Perm,,,
Timing,DV,EPOCH,Epoch,Char,EPOCH,"Epoch associated with the start date/time of the deviation. Examples: ""TREATMENT"", ""SCREENING"", ""FOLLOW-UP"".",12,Events,Perm,(EPOCH),,
Timing,DV,DVSTDTC,Start Date/Time of Deviation,Char,STDTC,Start date/time of deviation represented in ISO 8601 character format.,13,Events,Perm,ISO 8601,DV,
Timing,DV,DVENDTC,End Date/Time of Deviation,Char,ENDTC,End date/time of deviation represented in ISO 8601 character format.,14,Events,Perm,ISO 8601,DV,
Timing,DV,DVSTDY,Study Day of Start of Deviation Event,Num,STDY,Study day of start of event relative to the sponsor-defined RFSTDTC.,15,Events,Perm,,DV,
Timing,DV,DVENDY,Study Day of End of Observation,Num,ENDY,Study day of end of event relative to the sponsor-defined RFSTDTC.,16,Events,Perm,,DV,
Identifier,HO,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Events,Req,,,
Identifier,HO,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Events,Req,HO,,
Identifier,HO,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product.,3,Events,Req,,,
Identifier,HO,HOSEQ,Sequence Number,Num,SEQ,Sequence Number given to ensure uniqueness of subject records within a domain. May be any valid number.,4,Events,Req,,HO,
Identifier,HO,HOGRPID,Group ID,Char,GRPID,Used to tie together a block of related records in a single domain for a subject.,5,Events,Perm,,HO,
Identifier,HO,HOREFID,Reference ID,Char,REFID,Internal or external healthcare encounter identifier.,6,Events,Perm,,HO,
Identifier,HO,HOSPID,Sponsor-Defined Identifier,Char,SPID,Sponsor-defined identifier. It may be preprinted on the CRF as an explicit line identifier or defined in the sponsor's operational database. Example: Line number on a Healthcare encounters page.,7,Events,Perm,,HO,
Topic,HO,HOTERM,Healthcare Encounter Term,Char,TERM,Verbatim or preprinted CRF term for the healthcare encounter.,8,Events,Req,,HO,
Synonym Qualifier,HO,HODECOD,Dictionary-Derived Term,Char,DECOD,Dictionary or sponsor-defined derived text description of HOTERM or the modified topic variable (HOMODIFY).,9,Events,Perm,,HO,
Grouping Qualifier,HO,HOCAT,Category for Healthcare Encounter,Char,CAT,Used to define a category of topic-related values.,10,Events,Perm,,HO,
Grouping Qualifier,HO,HOSCAT,Subcategory for Healthcare Encounter,Char,SCAT,A further categorization of HOCAT values.,11,Events,Perm,,HO,
Variable Qualifier,HO,HOPRESP,Pre-Specified Healthcare Encounter,Char,PRESP,"A value of ""Y"" indicates that this healthcare encounter event was pre-specified on the CRF. Values are null for spontaneously reported events (i.e., those collected as free-text verbatim terms).",12,Events,Perm,(NY),HO,
Record Qualifier,HO,HOOCCUR,Healthcare Encounter Occurrence,Char,OCCUR,"Used when the occurrence of specific healthcare encounters is solicited, to indicate whether or not an encounter occurred. Values are null for spontaneously reported events.",13,Events,Perm,(NY),HO,
Record Qualifier,HO,HOSTAT,Completion Status,Char,STAT,The status indicates that the pre-specified question was not answered.,14,Events,Perm,(ND),HO,
Record Qualifier,HO,HOREASND,Reason Healthcare Encounter Not Done,Char,REASND,Describes the reason data for a pre-specified event was not collected. Used in conjunction with HOSTAT when value is "NOT DONE".,15,Events,Perm,,HO,
Timing,HO,TAETORD,Planned Order of Element within Arm,Num,TAETORD,Number that gives the planned order of the Element within the Arm.,16,Events,Perm,,,
Timing,HO,EPOCH,Epoch,Char,EPOCH,"Epoch associated with the start date/time of the healthcare encounter. Examples: ""SCREENING"", ""TREATMENT"", ""FOLLOW-UP"".",17,Events,Perm,(EPOCH),,
Timing,HO,HODTC,Date/Time of Event Collection,Char,DTC,Collection date and time of the healthcare encounter.,18,Events,Perm,ISO 8601,HO,
Timing,HO,HOSTDTC,Start Date/Time of Healthcare Encounter,Char,STDTC,"Start date/time of the healthcare encounter (e.g., date of admission).",19,Events,Exp,ISO 8601,HO,
Timing,HO,HOENDTC,End Date/Time of Healthcare Encounter,Char,ENDTC,End date/time of the healthcare encounter (date of discharge).,20,Events,Perm,ISO 8601,HO,
Timing,HO,HODY,Study Day of Event Collection,Num,DY,Study day of event collection relative to the sponsor-defined RFSTDTC.,21,Events,Perm,,HO,
Timing,HO,HOSTDY,Study Day of Start of Encounter,Num,STDY,Study day of the start of the healthcare encounter relative to the sponsor-defined RFSTDTC.,22,Events,Perm,,HO,
Timing,HO,HOENDY,Study Day of End of Healthcare Encounter,Num,ENDY,Study day of the end of the healthcare encounter relative to the sponsor-defined RFSTDTC.,23,Events,Perm,,HO,
Timing,HO,HODUR,Duration of Healthcare Encounter,Char,DUR,"Collected duration of the healthcare encounter. Used only if collected on the CRF and not derived from the start and end date/times. Example: P1DT2H (for 1 day, 2 hours).",24,Events,Perm,ISO 8601,HO,
Timing,HO,HOSTRTPT,Start Relative to Reference Time Point,Char,STRTPT,"Identifies the start of the observation as being before or after the sponsor-defined reference time point defined by variable --STTPT. \n Not all values of the codelist are allowable for this variable. See Section 4.4.7, Use of Relative Timing Variables.",25,Events,Perm,(STENRF),HO,
Timing,HO,HOSTTPT,Start Reference Time Point,Char,STTPT,Description or date/time in ISO 8601 character format of the sponsor-defined reference point referred to by STRTPT. Examples: "2003-12-15" or "VISIT 1".,26,Events,Perm,,HO,
Timing,HO,HOENRTPT,End Relative to Reference Time Point,Char,ENRTPT,"Identifies the end of the event as being before or after the reference time point defined by variable HOENTPT. \n Not all values of the codelist are allowable for this variable. See Section 4.4.7, Use of Relative Timing Variables.",27,Events,Perm,(STENRF),HO,
Timing,HO,HOENTPT,End Reference Time Point,Char,ENTPT,Description or date/time in ISO 8601 character format of the reference point referred to by HOENRTPT. Examples: "2003-12-25" or "VISIT 2".,28,Events,Perm,,HO,
Identifier,MH,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Events,Req,,,
Identifier,MH,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Events,Req,MH,,
Identifier,MH,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product.,3,Events,Req,,,
Identifier,MH,MHSEQ,Sequence Number,Num,SEQ,Sequence Number given to ensure uniqueness of subject records within a domain. May be any valid number.,4,Events,Req,,MH,
Identifier,MH,MHGRPID,Group ID,Char,GRPID,Used to tie together a block of related records in a single domain for a subject.,5,Events,Perm,,MH,
Identifier,MH,MHREFID,Reference ID,Char,REFID,Internal or external medical history identifier.,6,Events,Perm,,MH,
Identifier,MH,MHSPID,Sponsor-Defined Identifier,Char,SPID,Sponsor-defined reference number. Perhaps preprinted on the CRF as an explicit line identifier or defined in the sponsor's operational database. Example: Line number on a Medical History page.,7,Events,Perm,,MH,
Topic,MH,MHTERM,Reported Term for the Medical History,Char,TERM,Verbatim or preprinted CRF term for the medical condition or event.,8,Events,Req,,MH,
Synonym Qualifier,MH,MHMODIFY,Modified Reported Term,Char,MODIFY,"If MHTERM is modified to facilitate coding, then MHMODIFY will contain the modified text.",9,Events,Perm,,MH,
Synonym Qualifier,MH,MHDECOD,Dictionary-Derived Term,Char,DECOD,Dictionary-derived text description of MHTERM or MHMODIFY. Equivalent to the Preferred Term (PT in MedDRA). The sponsor is expected to provide the dictionary name and version used to map the terms utilizing the external codelist element in the Define-XML document.,10,Events,Perm,,MH,
Variable Qualifier,MH,MHEVDTYP,Medical History Event Date Type,Char,EVDTYP,"Specifies the aspect of the medical condition or event by which MHSTDTC and/or the MHENDTC is defined. Examples: &quot;DIAGNOSIS&quot;, &quot;SYMPTOMS&quot;, &quot;RELAPSE&quot;, &quot;INFECTION&quot;.",11,Events,Perm,(MHEDTTYP),MH,
Grouping Qualifier,MH,MHCAT,Category for Medical History,Char,CAT,Used to define a category of related records. Examples: &quot;CARDIAC&quot; or &quot;GENERAL&quot;.,12,Events,Perm,,MH,
Grouping Qualifier,MH,MHSCAT,Subcategory for Medical History,Char,SCAT,A further categorization of the condition or event.,13,Events,Perm,,MH,
Variable Qualifier,MH,MHPRESP,Medical History Event Pre-Specified,Char,PRESP,"A value of &quot;Y&quot; indicates that this medical history event was pre-specified on the CRF. Values are null for spontaneously reported events (i.e., those collected as free-text verbatim terms).",14,Events,Perm,(NY),MH,
Record Qualifier,MH,MHOCCUR,Medical History Occurrence,Char,OCCUR,"Used when the occurrence of specific medical history conditions is solicited, to indicate whether or not (&quot;Y&quot;/&quot;N&quot;) a medical condition (MHTERM) had ever occurred. Values are null for spontaneously reported events.",15,Events,Perm,(NY),MH,
Record Qualifier,MH,MHSTAT,Completion Status,Char,STAT,The status indicates that the pre-specified question was not asked/answered.,16,Events,Perm,(ND),MH,
Record Qualifier,MH,MHREASND,Reason Medical History Not Collected,Char,REASND,Describes the reason why data for a pre-specified condition was not collected. Used in conjunction with MHSTAT when value is &quot;NOT DONE&quot;.,17,Events,Perm,,MH,
Record Qualifier,MH,MHBODSYS,Body System or Organ Class,Char,BODSYS,"Dictionary-derived. Body system or organ class that is involved in an event or measurement from a standard hierarchy (e.g., MedDRA). When using a multi-axial dictionary such as MedDRA, this should contain the SOC used for the sponsor's analyses and summary tables which may not necessarily be the primary SOC.",18,Events,Perm,,MH,
Timing,MH,TAETORD,Planned Order of Element within Arm,Num,TAETORD,Number that gives the planned order of the Element within the Arm for the Element in which the assessment was made.,19,Events,Perm,,,
Timing,MH,EPOCH,Epoch,Char,EPOCH,Epoch associated with the start date/time of the medical history event.,20,Events,Perm,(EPOCH),,
Timing,MH,MHDTC,Date/Time of History Collection,Char,DTC,Collection date and time of the medical history observation represented in ISO 8601 character format.,21,Events,Perm,ISO 8601,MH,
Timing,MH,MHSTDTC,Start Date/Time of Medical History Event,Char,STDTC,Start date/time of the medical history event represented in ISO 8601 character format.,22,Events,Perm,ISO 8601,MH,
Timing,MH,MHENDTC,End Date/Time of Medical History Event,Char,ENDTC,End date/time of the medical history event.,23,Events,Perm,ISO 8601,MH,
Timing,MH,MHDY,Study Day of History Collection,Num,DY,"1. Study day of medical history collection, measured as integer days. \n 2. Algorithm for calculations must be relative to the sponsor-defined RFSTDTC variable in Demographics. This formula should be consistent across the submission.",24,Events,Perm,,MH,
Timing,MH,MHENRF,End Relative to Reference Period,Char,ENRF,"Describes the end of the event relative to the sponsor-defined reference period. The sponsor-defined reference period is a continuous period of time defined by a discrete starting point and a discrete ending point (represented by RFSTDTC and RFENDTC in Demographics). \n Not all values of the codelist are allowable for this variable. See Section 4.4.7, Use of Relative Timing Variables.",25,Events,Perm,(STENRF),MH,
Timing,MH,MHENRTPT,End Relative to Reference Time Point,Char,ENRTPT,"Identifies the end of the event as being before or after the reference time point defined by variable MHENTPT. \n Not all values of the codelist are allowable for this variable. See Section 4.4.7, Use of Relative Timing Variables.",26,Events,Perm,(STENRF),MH,
Timing,MH,MHENTPT,End Reference Time Point,Char,ENTPT,Description or date/time in ISO 8601 character format of the reference point referred to by MHENRTPT. Examples: &quot;2003-12-25&quot; or &quot;VISIT 2&quot;.,27,Events,Perm,,MH,
Identifier,CV,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Findings,Req,,,
Identifier,CV,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Findings,Req,CV,,
Identifier,CV,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product.,3,Findings,Req,,,
Identifier,CV,CVSEQ,Sequence Number,Num,SEQ,Sequence number to ensure uniqueness of records within a dataset for a subject. May be any valid number (including decimals) and does not have to start at 1.,4,Findings,Req,,CV,
Identifier,CV,CVGRPID,Group ID,Char,GRPID,"Optional group identifier, used to link together a block of related records within a subject in a domain.",5,Findings,Perm,,CV,
Identifier,CV,CVREFID,Reference ID,Char,REFID,Optional internal or external identifier.,6,Findings,Perm,,CV,
Identifier,CV,CVSPID,Sponsor-Defined Identifier,Char,SPID,Sponsor-defined identifier. Example: &quot;preprinted line identifier on a Case Report Form&quot;.,7,Findings,Perm,,CV,
Identifier,CV,CVLNKID,Link ID,Char,LNKID,Identifier used to link related records across domains. This may be a one-to-one or a one-to-many relationship.,8,Findings,Perm,,CV,
Identifier,CV,CVLNKGRP,Link Group,Char,LNKGRP,Identifier used to link related records across domains. This will usually be a many-to-one relationship.,9,Findings,Perm,,CV,
Topic,CV,CVTESTCD,Short Name of Cardiovascular Test,Char,TESTCD,"Short name of the measurement, test, or examination described in CVTEST. It can be used as a column name when converting a dataset from a vertical to a horizontal format. The value in CVTESTCD cannot be longer than 8 characters, nor can it start with a number (e.g., &quot;1TEST&quot;). CVTESTCD cannot contain characters other than letters, numbers, or underscores.",10,Findings,Req,(CVTESTCD),CV,
Synonym Qualifier,CV,CVTEST,Name of Cardiovascular Test,Char,TEST,Long name For CVTESTCD. The value in CVTEST cannot be longer than 40 characters.,11,Findings,Req,(CVTEST),CV,
Grouping Qualifier,CV,CVCAT,Category for Cardiovascular Test,Char,CAT,Used to define a category of topic-variable values.,12,Findings,Perm,,CV,
Grouping Qualifier,CV,CVSCAT,Subcategory for Cardiovascular Test,Char,SCAT,Used to define a further categorization of CVCAT values.,13,Findings,Perm,,CV,
Record Qualifier,CV,CVPOS,Position of Subject During Observation,Char,POS,"Position of the subject during a measurement or examination. Examples: &quot;SUPINE&quot;, &quot;STANDING&quot;, &quot;SITTING&quot;.",14,Findings,Perm,(POSITION),CV,
Result Qualifier,CV,CVORRES,Result or Finding in Original Units,Char,ORRES,Result of the measurement or finding as originally received or collected.,15,Findings,Exp,,CV,
Variable Qualifier,CV,CVORRESU,Original Units,Char,ORRESU,Original units in which the data were collected. Unit for CVORRES.,16,Findings,Perm,(UNIT),CV,
Result Qualifier,CV,CVSTRESC,Character Result/Finding in Std Format,Char,STRESC,"Contains the result value for all findings, copied or derived from CVORRES in a standard format or in standard units. CVSTRESC should store all results or findings in character format; if results are numeric, they should also be stored in numeric format in CVSTRESN. For example, if various tests have results &quot;NONE&quot;, &quot;NEG&quot;, and &quot;NEGATIVE&quot; in CVORRES and these results effectively have the same meaning, they could be represented in standard format in CVSTRESC as &quot;NEGATIVE&quot;.",17,Findings,Exp,,CV,
Result Qualifier,CV,CVSTRESN,Numeric Result/Finding in Standard Units,Num,STRESN,Used for continuous or numeric results or findings in standard format; copied in numeric format from CVSTRESC. CVSTRESN should store all numeric test results or findings.,18,Findings,Perm,,CV,
Variable Qualifier,CV,CVSTRESU,Standard Units,Char,STRESU,Standardized units used for CVSTRESC and CVSTRESN.,19,Findings,Perm,(UNIT),CV,
Record Qualifier,CV,CVSTAT,Completion Status,Char,STAT,"Used to indicate that a question was not asked or a test was not done, or a test was attempted but did not generate a result. Should be null or have a value of &quot;NOT DONE&quot;.",20,Findings,Perm,(ND),CV,
Record Qualifier,CV,CVREASND,Reason Not Done,Char,REASND,Describes why a measurement or test was not performed. Examples: &quot;BROKEN EQUIPMENT&quot; or &quot;SUBJECT REFUSED&quot;. Used in conjunction with CVSTAT when value is &quot;NOT DONE&quot;.,21,Findings,Perm,,CV,
Record Qualifier,CV,CVLOC,Location Used for the Measurement,Char,LOC,"Anatomical location of the subject relevant to the collection of the measurement. Example: &quot;HEART&quot;, &quot;LEFT VENTRICLE&quot;.",22,Findings,Perm,(LOC),CV,
Variable Qualifier,CV,CVLAT,Laterality,Char,LAT,"Qualifier for anatomical location or specimen further detailing laterality. Examples: &quot;RIGHT&quot;, &quot;LEFT&quot;, &quot;BILATERAL&quot;, &quot;UNILATERAL&quot;.",23,Findings,Perm,(LAT),CV,
Variable Qualifier,CV,CVDIR,Directionality,Char,DIR,"Qualifier for anatomical location or specimen further detailing directionality. Examples: &quot;ANTERIOR&quot;, &quot;LOWER&quot;, &quot;PROXIMAL&quot;.",24,Findings,Perm,(DIR),CV,
Record Qualifier,CV,CVMETHOD,Method of Test or Examination,Char,METHOD,Method used to create the result.,25,Findings,Perm,(METHOD),CV,
Record Qualifier,CV,CVLOBXFL,Last Observation Before Exposure Flag,Char,LOBXFL,Operationally-derived indicator used to identify the last non-missing value prior to RFXSTDTC. The value should be &quot;Y&quot; or null.,26,Findings,Exp,(NY),CV,
Record Qualifier,CV,CVBLFL,Baseline Flag,Char,BLFL,Indicator used to identify a baseline value. Should be &quot;Y&quot; or null. Note that CVBLFL is retained for backward compatibility. The authoritative baseline for statistical analysis is in an ADaM dataset.,27,Findings,Perm,(NY),CV,
Record Qualifier,CV,CVDRVFL,Derived Flag,Char,DRVFL,"Used to indicate a derived record (e.g., a record that represents the average of other records such as a computed baseline). Should be &quot;Y&quot; or null.",28,Findings,Perm,(NY),CV,
Record Qualifier,CV,CVEVAL,Evaluator,Char,EVAL,"Role of the person who provided the evaluation. Used only for results that are subjective (e.g., assigned by a person or a group). Examples: &quot;ADJUDICATION COMMITTEE&quot;, &quot; INDEPENDENT ASSESSOR&quot;, &quot;RADIOLOGIST&quot;.",29,Findings,Perm,(EVAL),CV,
Variable Qualifier,CV,CVEVALID,Evaluator Identifier,Char,EVALID,Used to distinguish multiple evaluators with the same role recorded in CVEVAL. Examples: &quot;RADIOLOGIST1&quot; or &quot;RADIOLOGIST2&quot;.,30,Findings,Perm,(MEDEVAL),CV,
Timing,CV,VISITNUM,Visit Number,Num,VISITNUM,"1. Clinical encounter number. \n 2. Numeric version of VISIT, used for sorting.",31,Findings,Exp,,,
Timing,CV,VISIT,Visit Name,Char,VISIT,Protocol-defined description of clinical encounter. May be used in addition to VISITNUM and/or VISITDY.,32,Findings,Perm,,,
Timing,CV,VISITDY,Planned Study Day of Visit,Num,VISITDY,Planned study day of VISIT. Should be an integer.,33,Findings,Perm,,,
Timing,CV,TAETORD,Planned Order of Element within Arm,Num,TAETORD,Number that gives the planned order of the Element within the Arm for the element in which the assessment was made.,34,Findings,Perm,,,
Timing,CV,EPOCH,Epoch,Char,EPOCH,Epoch associated with the date/time at which the assessment was made.,35,Findings,Perm,(EPOCH),,
Timing,CV,CVDTC,Date/Time of Test,Char,DTC,Collection date and time of an observation.,36,Findings,Exp,ISO 8601,CV,
Timing,CV,CVDY,Study Day of Visit/Collection/Exam,Num,DY,Actual study day of visit/collection/exam expressed in integer days relative to the sponsor-defined RFSTDTC in Demographics.,37,Findings,Perm,,CV,
Timing,CV,CVTPT,Planned Time Point Name,Char,TPT,"Text description of time when a measurement or observation should be taken, as defined in the protocol. This may be represented as an elapsed time relative to a fixed reference point, such as time of last dose. See CVTPTNUM and CVTPTREF.",38,Findings,Perm,,CV,
Timing,CV,CVTPTNUM,Planned Time Point Number,Num,TPTNUM,Numeric version of planned time point used in sorting.,39,Findings,Perm,,CV,
Timing,CV,CVELTM,Planned Elapsed Time from Time Point Ref,Char,ELTM,"Planned Elapsed time relative to a planned fixed reference (CVTPTREF) such as &quot;PREVIOUS DOSE&quot; or &quot;PREVIOUS MEAL&quot;. This variable is useful where there are repetitive measures. Not a clock time or a date/time variable, but an interval, represented as ISO duration.",40,Findings,Perm,ISO 8601,CV,
Timing,CV,CVTPTREF,Time Point Reference,Char,TPTREF,"Description of the fixed reference point referred to by CVELTM, CVTPTNUM, and CVTPT. Examples: &quot;PREVIOUS DOSE&quot;, &quot;PREVIOUS MEAL&quot;.",41,Findings,Perm,,CV,
Timing,CV,CVRFTDTC,Date/Time of Reference Time Point,Char,RFTDTC,Date/time for a fixed reference time point defined by CVTPTREF.,42,Findings,Perm,ISO 8601,CV,
Identifier,DA,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study within the submission.,1,Findings,Req,,,
Identifier,DA,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Findings,Req,DA,,
Identifier,DA,USUBJID,Unique Subject Identifier,Char,USUBJID,Unique subject identifier within the submission.,3,Findings,Req,,,
Identifier,DA,DASEQ,Sequence Number,Num,SEQ,Sequence number given to ensure uniqueness of subject records within a domain. May be any valid number.,4,Findings,Req,,DA,
Identifier,DA,DAGRPID,Group ID,Char,GRPID,Used to tie together a block of related records in a single domain for a subject.,5,Findings,Perm,,DA,
Identifier,DA,DAREFID,Reference ID,Char,REFID,Internal or external identifier such as label number.,6,Findings,Perm,,DA,
Identifier,DA,DASPID,Sponsor-Defined Identifier,Char,SPID,"Sponsor-defined reference number. Perhaps preprinted on the CRF as an explicit line identifier or defined in the sponsor's operational database. Examples: Line number on the Drug Accountability page, drug label code.",7,Findings,Perm,,DA,
Topic,DA,DATESTCD,Short Name of Accountability Assessment,Char,TESTCD,"Short character value for DATEST used as a column name when converting a dataset from a vertical format to a horizontal format. The short value can be up to 8 characters and cannot begin with a number or contain characters other than letters, numbers, or underscores. Example: &quot;DISPAMT&quot;, &quot;RETAMT&quot;.",8,Findings,Req,(DATESTCD),DA,
Synonym Qualifier,DA,DATEST,Name of Accountability Assessment,Char,TEST,"Verbatim name, corresponding to the topic variable, of the test or examination used to obtain the drug accountability assessment. The value in DATEST cannot be longer than 40 characters. Example: &quot;Dispensed Amount&quot;, &quot;Returned Amount&quot;.",9,Findings,Req,(DATEST),DA,
Grouping Qualifier,DA,DACAT,Category,Char,CAT,"Used to define a category of topic-variable values. Examples: &quot;STUDY MEDICATION&quot;, &quot;RESCUE MEDICATION&quot;.",10,Findings,Perm,,DA,
Grouping Qualifier,DA,DASCAT,Subcategory,Char,SCAT,Used to define a further categorization level for a group of related records.,11,Findings,Perm,,DA,
Result Qualifier,DA,DAORRES,Result or Finding in Original Units,Char,ORRES,Result of the Drug Accountability assessment as originally received or collected.,12,Findings,Exp,,DA,
Variable Qualifier,DA,DAORRESU,Original Units,Char,ORRESU,Unit for DAORRES.,13,Findings,Perm,(UNIT),DA,
Result Qualifier,DA,DASTRESC,Result or Finding in Standard Format,Char,STRESC,"Contains the result value for all Drug Accountability assessments, copied or derived from DAORRES in a standard format or in standard units. DASTRESC should store all results or findings in character format; if results are numeric, they should also be stored in numeric format in DASTRESN.",14,Findings,Exp,,DA,
Result Qualifier,DA,DASTRESN,Numeric Result/Finding in Standard Units,Num,STRESN,Used for continuous or numeric results or findings in standard format; copied in numeric format from DASTRESC. DASTRESN should store all numeric test results or findings.,15,Findings,Perm,,DA,
Variable Qualifier,DA,DASTRESU,Standard Units,Char,STRESU,Standardized units used for DASTRESC and DASTRESN.,16,Findings,Perm,(UNIT),DA,
Record Qualifier,DA,DASTAT,Completion Status,Char,STAT,Used to indicate that a drug accountability assessment was not done. Should be null or have a value of &quot;NOT DONE&quot;.,17,Findings,Perm,(ND),DA,
Record Qualifier,DA,DAREASND,Reason Not Done,Char,REASND,Reason not done. Used in conjunction with DASTAT when value is &quot;NOT DONE&quot;.,18,Findings,Perm,,DA,
Timing,DA,VISITNUM,Visit Number,Num,VISITNUM,"1. Clinical encounter number. \n 2. Numeric version of VISIT, used for sorting.",19,Findings,Exp,,,
Timing,DA,VISIT,Visit Name,Char,VISIT,Protocol-defined description of a clinical encounter.May be used in addition to VISITNUM and/or VISITDY.,20,Findings,Perm,,,
Timing,DA,VISITDY,Planned Study Day of Visit,Num,VISITDY,"Planned study day of the visit, based upon RFSTDTC in Demographics.",21,Findings,Perm,,,
Timing,DA,TAETORD,Planned Order of Element within Arm,Num,TAETORD,Number that gives the planned order of the Element within the Arm.,22,Findings,Perm,,,
Timing,DA,EPOCH,Epoch,Char,EPOCH,"Epoch associated with the start date/time of the observation, or the date/time of collection if start date/time is not collected.",23,Findings,Perm,(EPOCH),,
Timing,DA,DADTC,Date/Time of Collection,Char,DTC,Date and time of the drug accountability assessment represented in ISO 8601 character format.,24,Findings,Exp,ISO 8601,DA,
Timing,DA,DADY,Study Day of Visit/Collection/Exam,Num,DY,"Study day of drug accountability assessment, measured in integer days.Algorithm for calculations must be relative to the sponsor-defined RFSTDTC in Demographics.",25,Findings,Perm,,DA,
Identifier,DD,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Findings,Req,,,
Identifier,DD,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Findings,Req,DD,,
Identifier,DD,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product.,3,Findings,Req,,,
Identifier,DD,DDSEQ,Sequence Number,Num,SEQ,Sequence number given to ensure uniqueness of subject records within a domain. May be any valid number.,4,Findings,Req,,DD,
Topic,DD,DDTESTCD,Death Detail Assessment Short Name,Char,TESTCD,"Short name of the measurement, test, or examination described in DDTEST. It can be used as a column name when converting a dataset from a vertical to a horizontal format. The value in DDTESTCD cannot be longer than 8 characters, nor can it start with a number (e.g., ""1TEST"" is not valid). DDTESTCD cannot contain characters other than letters, numbers, or underscores. Examples: ""PRCDTH"", ""SECDTH"".",5,Findings,Req,(DTHDXCD),DD,
Synonym Qualifier,DD,DDTEST,Death Detail Assessment Name,Char,TEST,"Long name for DDTESTCD. The value in DDTEST cannot be longer than 40 characters. Examples: ""Primary Cause of Death"", ""Secondary Cause of Death"".",6,Findings,Req,(DTHDX),DD,
Result Qualifier,DD,DDORRES,Result or Finding as Collected,Char,ORRES,"Result of the test defined in DDTEST, as originally received or collected.",7,Findings,Exp,,DD,
Result Qualifier,DD,DDSTRESC,Character Result/Finding in Std Format,Char,STRESC,Contains the result or finding copied or derived from DDORRES in a standard format.,8,Findings,Exp,,DD,
Variable Qualifier,DD,DDRESCAT,Result Category,Char,RESCAT,"Used to categorize the result of a finding. Examples: ""TREATMENT RELATED"", ""NONTREATMENT RELATED"", ""UNDETERMINED"", ""ACCIDENTAL"".",9,Findings,Perm,,DD,
Record Qualifier,DD,DDEVAL,Evaluator,Char,EVAL,Role of the person who provided the evaluation.,10,Findings,Perm,(EVAL),DD,
Timing,DD,DDDTC,Date/Time of Collection,Char,DTC,Date/time of collection of the diagnosis or other death assessment data in ISO 8601 format. This is not necessarily the date of death.,11,Findings,Exp,ISO 8601,DD,
Timing,DD,DDDY,Study Day of Collection,Num,DY,"Study day of the collection, in integer days. The algorithm for calculations must be relative to the sponsor-defined RFSTDTC variable in the Demographics (DM) domain.",12,Findings,Perm,,DD,
Identifier,EG,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Findings,Req,,,
Identifier,EG,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Findings,Req,EG,,
Identifier,EG,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product.,3,Findings,Req,,,
Identifier,EG,SPDEVID,Sponsor Device Identifier,Char,SPDEVID,Sponsor-defined identifier for a device.,4,Findings,Perm,,,
Identifier,EG,EGSEQ,Sequence Number,Num,SEQ,Sequence number given to ensure uniqueness of subject records within a domain. May be any valid number.,5,Findings,Req,,EG,
Identifier,EG,EGGRPID,Group ID,Char,GRPID,Used to tie together a block of related records in a single domain for a subject.,6,Findings,Perm,,EG,
Identifier,EG,EGREFID,ECG Reference ID,Char,REFID,Internal or external ECG identifier. Example: &quot;UUID&quot;.,7,Findings,Perm,,EG,
Identifier,EG,EGSPID,Sponsor-Defined Identifier,Char,SPID,Sponsor-defined reference number. Perhaps preprinted on the CRF as an explicit line identifier or defined in the sponsor's operational database. Example: Line number from the ECG page.,8,Findings,Perm,,EG,
Topic,EG,EGTESTCD,ECG Test or Examination Short Name,Char,TESTCD,"Short name of the measurement, test, or examination described in EGTEST. It can be used as a column name when converting a dataset from a vertical to a horizontal format. The value in EGTESTCD cannot be longer than 8 characters, nor can it start with a number (e.g., &quot;1TEST&quot; is not valid). EGTESTCD cannot contain characters other than letters, numbers, or underscores. Examples : &quot;PRAG&quot;, &quot;QRSAG&quot;. \n Test codes are in two separate codelists, one for tests based on regular 10-second ECGs (EGTESTCD) and one for tests based on Holter monitoring (HETESTCD).",9,Findings,Req,(EGTESTCD)(HETESTCD),EG,
Synonym Qualifier,EG,EGTEST,ECG Test or Examination Name,Char,TEST,"Verbatim name of the test or examination used to obtain the measurement or finding. The value in EGTEST cannot be longer than 40 characters. Examples: &quot;PR Interval, Aggregate&quot;, &quot;QRS Duration, Aggregate&quot;. \n Test names are in two separate codelists, one for tests based on regular 10-second ECGs (EGTEST) and one for tests based on Holter monitoring (HETEST).",10,Findings,Req,(EGTEST)(HETEST),EG,
Grouping Qualifier,EG,EGCAT,Category for ECG,Char,CAT,"Used to categorize ECG observations across subjects. Examples: &quot;MEASUREMENT&quot;, &quot;FINDING&quot;, &quot;INTERVAL&quot;.",11,Findings,Perm,,EG,
Grouping Qualifier,EG,EGSCAT,Subcategory for ECG,Char,SCAT,A further categorization of the ECG.,12,Findings,Perm,,EG,
Record Qualifier,EG,EGPOS,ECG Position of Subject,Char,POS,"Position of the subject during a measurement or examination. Examples: &quot;SUPINE&quot;, &quot;STANDING&quot;, &quot;SITTING&quot;.",13,Findings,Perm,(POSITION),EG,
Variable Qualifier,EG,EGBEATNO,ECG Beat Number,Num,BEATNO,A sequence number that identifies the beat within an ECG.,14,Findings,Perm,,EG,
Result Qualifier,EG,EGORRES,Result or Finding in Original Units,Char,ORRES,"Result of the ECG measurement or finding as originally received or collected. Examples of expected values are &quot;62&quot; or &quot;0.151&quot; when the result is an interval or measurement, or &quot;ATRIAL FIBRILLATION&quot; or &quot;QT PROLONGATION&quot; when the result is a finding.",15,Findings,Exp,,EG,
Variable Qualifier,EG,EGORRESU,Original Units,Char,ORRESU,Original units in which the data were collected. The unit for EGORRES. Examples: &quot;sec&quot; or &quot;msec&quot;.,16,Findings,Perm,(UNIT),EG,
Result Qualifier,EG,EGSTRESC,Character Result/Finding in Std Format,Char,STRESC,"Contains the result value for all findings, copied or derived from EGORRES in a standard format or standard units. EGSTRESC should store all results or findings in character format; if results are numeric, they should also be stored in numeric format in EGSTRESN. For example, if a test has results of &quot;NONE&quot;, &quot;NEG&quot;, and &quot;NEGATIVE&quot; in EGORRES and these results effectively have the same meaning, they could be represented in standard format in EGSTRESC as &quot;NEGATIVE&quot;. For other examples, see general assumptions. Additional examples of result data: &quot;SINUS BRADYCARDIA&quot;, &quot;ATRIAL FLUTTER&quot;, &quot;ATRIAL FIBRILLATION&quot;. \n Test results are in two separate codelists, one for tests based on regular 10-second ECGs (EGSTRESC) and one for tests based on Holter monitoring (HESTRESC).",17,Findings,Exp,(EGSTRESC)(HESTRESC),EG,
Result Qualifier,EG,EGSTRESN,Numeric Result/Finding in Standard Units,Num,STRESN,Used for continuous or numeric results or findings in standard format; copied in numeric format from EGSTRESC. EGSTRESN should store all numeric test results or findings.,18,Findings,Perm,,EG,
Variable Qualifier,EG,EGSTRESU,Standard Units,Char,STRESU,Standardized units used for EGSTRESC and EGSTRESN.,19,Findings,Perm,(UNIT),EG,
Record Qualifier,EG,EGSTAT,Completion Status,Char,STAT,"Used to indicate an ECG was not done, or an ECG measurement was not taken. Should be null if a result exists in EGORRES.",20,Findings,Perm,(ND),EG,
Record Qualifier,EG,EGREASND,Reason ECG Not Done,Char,REASND,Describes why a measurement or test was not performed. Examples: &quot;BROKEN EQUIPMENT&quot; or &quot;SUBJECT REFUSED&quot;. Used in conjunction with EGSTAT when value is &quot;NOT DONE&quot;.,21,Findings,Perm,,EG,
Record Qualifier,EG,EGXFN,ECG External File Path,Char,XFN,File name and path for the external ECG waveform file.,22,Findings,Perm,,EG,
Record Qualifier,EG,EGNAM,Vendor Name,Char,NAM,Name or identifier of the laboratory or vendor who provided the test results.,23,Findings,Perm,,EG,
Record Qualifier,EG,EGMETHOD,Method of Test or Examination,Char,METHOD,Method of the ECG test. Example: &quot;12 LEAD STANDARD&quot;.,24,Findings,Perm,(EGMETHOD),EG,
Record Qualifier,EG,EGLEAD,Lead Location Used for Measurement,Char,LEAD,"The lead used for the measurement. Examples: &quot;LEAD 1&quot;, &quot;LEAD 2&quot;, &quot;LEAD 3&quot;, &quot;LEAD rV2&quot;, &quot;LEAD V1&quot;.",25,Findings,Perm,(EGLEAD),EG,
Record Qualifier,EG,EGLOBXFL,Last Observation Before Exposure Flag,Char,LOBXFL,Operationally-derived indicator used to identify the last non-missing value prior to RFXSTDTC. The value should be &quot;Y&quot; or null.,26,Findings,Exp,(NY),EG,
Record Qualifier,EG,EGBLFL,Baseline Flag,Char,BLFL,Indicator used to identify a baseline value. Should be &quot;Y&quot; or null. Note that EGBLFL is retained for backward compatibility. The authoritative baseline for statistical analysis is in an ADaM dataset.,27,Findings,Perm,(NY),EG,
Record Qualifier,EG,EGDRVFL,Derived Flag,Char,DRVFL,"Used to indicate a derived record. The value should be &quot;Y&quot; or null. Records that represent the average of other records, or that do not come from the CRF, or are not as originally collected or received are examples of records that would be derived for the submission datasets. If EGDRVFL = &quot;Y&quot;, then EGORRES could be null, with EGSTRESC and EGSTRESN (if the result is numeric) having the derived value.",28,Findings,Perm,(NY),EG,
Record Qualifier,EG,EGEVAL,Evaluator,Char,EVAL,"Role of the person who provided the evaluation. Used only for results that are subjective (e.g., assigned by a person or a group). Should be null for records that contain collected or derived data. Examples: &quot;INVESTIGATOR&quot;, &quot;ADJUDICATION COMMITTEE&quot;, &quot;VENDOR&quot;.",29,Findings,Perm,(EVAL),EG,
Variable Qualifier,EG,EGEVALID,Evaluator Identifier,Char,EVALID,Used to distinguish multiple evaluators with the same role recorded in EGEVAL. Examples: &quot;RADIOLOGIST 1&quot; or &quot;RADIOLOGIST 2&quot;.,30,Findings,Perm,(MEDEVAL),EG,
Record Qualifier,EG,EGREPNUM,Repetition Number,Num,REPNUM,"The incidence number of a test that is repeated within a given timeframe for the same test. The level of granularity can vary, e.g., within a time point or within a visit. For example, multiple measurements of blood pressure or multiple analyses of a sample.",31,Findings,Perm,,EG,
Timing,EG,VISITNUM,Visit Number,Num,VISITNUM,"1. Clinical encounter number. \n 2. Numeric version of VISIT, used for sorting.",32,Findings,Exp,,,
Timing,EG,VISIT,Visit Name,Char,VISIT,Protocol-defined description of clinical encounter.May be used in addition to VISITNUM and/or VISITDY.,33,Findings,Perm,,,
Timing,EG,VISITDY,Planned Study Day of Visit,Num,VISITDY,Planned study day of the visit based upon RFSTDTC in Demographics.,34,Findings,Perm,,,
Timing,EG,TAETORD,Planned Order of Element within Arm,Num,TAETORD,Number that gives the planned order of the Element within the Arm for the element in which the assessment was made.,35,Findings,Perm,,,
Timing,EG,EPOCH,Epoch,Char,EPOCH,Epoch associated with the date/time at which the assessment was made.,36,Findings,Perm,(EPOCH),,
Timing,EG,EGDTC,Date/Time of ECG,Char,DTC,Date/Time of ECG.,37,Findings,Exp,ISO 8601,EG,
Timing,EG,EGDY,Study Day of ECG,Num,DY,"Study day of the ECG, measured as integer days.Algorithm for calculations must be relative to the sponsor-defined RFSTDTC variable in Demographics.",38,Findings,Perm,,EG,
Timing,EG,EGTPT,Planned Time Point Name,Char,TPT,"Text description of time when measurement should be taken.This may be represented as an elapsed time relative to a fixed reference point, such as time of last dose. See EGTPTNUM and EGTPTREF. Examples: &quot;Start&quot;, &quot;5 min post&quot;.",39,Findings,Perm,,EG,
Timing,EG,EGTPTNUM,Planned Time Point Number,Num,TPTNUM,Numerical version of EGTPT to aid in sorting.,40,Findings,Perm,,EG,
Timing,EG,EGELTM,Planned Elapsed Time from Time Point Ref,Char,ELTM,"Planned elapsed time (in ISO 8601) relative to a fixed time point reference (EGTPTREF). Not a clock time or a date time variable. Represented as an ISO 8601 duration. Examples: &quot;-PT15M&quot; to represent the period of 15 minutes prior to the reference point indicated by EGTPTREF, or &quot;PT8H&quot; to represent the period of 8 hours after the reference point indicated by EGTPTREF.",41,Findings,Perm,ISO 8601,EG,
Timing,EG,EGTPTREF,Time Point Reference,Char,TPTREF,"Name of the fixed reference point referred to by EGELTM, EGTPTNUM, and EGTPT. Examples: &quot;PREVIOUS DOSE&quot;, &quot;PREVIOUS MEAL&quot;.",42,Findings,Perm,,EG,
Timing,EG,EGRFTDTC,Date/Time of Reference Time Point,Char,RFTDTC,Date/time for a fixed reference time point defined by EGTPTREF.,43,Findings,Perm,ISO 8601,EG,
Identifier,FT,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Findings,Req,,,
Identifier,FT,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Findings,Req,FT,,
Identifier,FT,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product.,3,Findings,Req,,,
Identifier,FT,FTSEQ,Sequence Number,Num,SEQ,Sequence number to ensure uniqueness of records within a dataset for a subject. May be any valid number.,4,Findings,Req,,FT,
Identifier,FT,FTGRPID,Group ID,Char,GRPID,"Optional group identifier, used to link together a block of related records within a subject in a domain.",5,Findings,Perm,,FT,
Identifier,FT,FTREFID,Reference ID,Char,REFID,Optional internal or external identifier.,6,Findings,Perm,,FT,
Identifier,FT,FTSPID,Sponsor-Defined Identifier,Char,SPID,Sponsor-defined identifier. Perhaps preprinted on the CRF as an explicit line identifier or defined in the sponsor's operational database. Example: Line number from the test page.,7,Findings,Perm,,FT,
Topic,FT,FTTESTCD,Short Name of Test,Char,TESTCD,"Short character value for FTTEST, which can be used as a column name when converting a dataset from a vertical format to a horizontal format. The value cannot be longer than 8 characters, nor can it start with a number (e.g., ""1TEST"" is not valid). FTTESTCD cannot contain characters other than letters, numbers, or underscores. \n Controlled terminology for FTTESTCD is published in separate codelists for each questionnaire. See https://www.cdisc.org/standards/semantics/terminology for values for FTTESTCD. Examples: ""W250101"", ""W25F0102"".",8,Findings,Req,,FT,
Synonym Qualifier,FT,FTTEST,Name of Test,Char,TEST,"Verbatim name of the question used to obtain the finding. The value in FTTEST cannot be longer than 40 characters. \n Controlled terminology for FTTEST is published in separate codelists for each questionnaire. See https://www.cdisc.org/standards/semantics/terminology for values for FTTEST. Examples: ""W2501-25 Foot Walk Time"", ""W25F-More Than Two Attempts"".",9,Findings,Req,,FT,
Grouping Qualifier,FT,FTCAT,Category,Char,CAT,Used to specify the functional test in which the functional test question identified by FTTEST and FTTESTCD was included.,10,Findings,Req,(FTCAT),FT,
Grouping Qualifier,FT,FTSCAT,Subcategory,Char,SCAT,Used to define a further categorization of FTCAT values.,11,Findings,Perm,,FT,
Record Qualifier,FT,FTPOS,Position of Subject During Observation,Char,POS,"Position of the subject during the test. Examples: ""SUPINE"", ""STANDING"", ""SITTING"".",12,Findings,Perm,(POSITION),FT,
Result Qualifier,FT,FTORRES,Result or Finding in Original Units,Char,ORRES,Result of the measurement or finding as originally received or collected.,13,Findings,Exp,,FT,
Variable Qualifier,FT,FTORRESU,Original Units,Char,ORRESU,Original units in which the data were collected. Unit for FTORRES.,14,Findings,Perm,(UNIT),FT,
Result Qualifier,FT,FTSTRESC,Result or Finding in Standard Format,Char,STRESC,"Contains the result value for all findings, copied or derived from FTORRES in a standard format or in standard units. FTSTRESC should store all results or findings in character format; if results are numeric, they should also be stored in numeric format in FTSTRESN.",15,Findings,Exp,,FT,
Result Qualifier,FT,FTSTRESN,Numeric Result/Finding in Standard Units,Num,STRESN,Used for continuous or numeric results or findings in standard format; copied in numeric format from FTSTRESC. FTSTRESN should store all numeric test results or findings.,16,Findings,Perm,,FT,
Variable Qualifier,FT,FTSTRESU,Standard Units,Char,STRESU,Standardized units used for FTSTRESC and FTSTRESN.,17,Findings,Perm,(UNIT),FT,
Record Qualifier,FT,FTSTAT,Completion Status,Char,STAT,"Used to indicate that a test was not done, or a test was attempted but did not generate a result. Should be null or have a value of ""NOT DONE"".",18,Findings,Perm,(ND),FT,
Record Qualifier,FT,FTREASND,Reason Not Done,Char,REASND,"Describes why a test was not done, or a test was attempted but did not generate a result. Used in conjunction with FTSTAT when value is ""NOT DONE"".",19,Findings,Perm,,FT,
Record Qualifier,FT,FTXFN,External File Path,Char,XFN,File path to an external file.,20,Findings,Perm,,FT,
Record Qualifier,FT,FTNAM,Vendor Name,Char,NAM,Name or identifier of the vendor or laboratory that provided the test results.,21,Findings,Perm,,FT,
Record Qualifier,FT,FTMETHOD,Method of Test,Char,METHOD,Method of the test.,22,Findings,Perm,(METHOD),FT,
Record Qualifier,FT,FTLOBXFL,Last Observation Before Exposure Flag,Char,LOBXFL,Operationally-derived indicator used to identify the last non-missing value prior to RFXSTDTC. The value should be "Y" or null.,23,Findings,Exp,(NY),FT,
Record Qualifier,FT,FTBLFL,Baseline Flag,Char,BLFL,"A baseline defined by the sponsor (could be derived in the same manner as FTLOBXFL or ABLFL, but is not required to be). The value should be ""Y"" or null. Note that FTBLFL is retained for backward compatibility. The authoritative baseline flag for statistical analysis is in an ADaM dataset.",24,Findings,Perm,(NY),FT,
Record Qualifier,FT,FTDRVFL,Derived Flag,Char,DRVFL,"Used to indicate a derived record (e.g., a record that represents the average of other records such as a computed baseline). Should be ""Y"" or null.",25,Findings,Perm,(NY),FT,
Record Qualifier,FT,FTEVAL,Evaluator,Char,EVAL,"Role of the person who provided the evaluation. Used only for results that are subjective (e.g., assigned by a person or a group). Examples: ""ADJUDICATION COMMITTEE"", ""INDEPENDENT ASSESSOR"", ""RADIOLOGIST"".",26,Findings,Perm,(EVAL),FT,
Record Qualifier,FT,FTREPNUM,Repetition Number,Num,REPNUM,"The incidence number of a test that is repeated within a given timeframe for the same test. The level of granularity can vary, e.g., within a time point or within a visit. For example, multiple measurements of blood pressure or multiple analyses of a sample.",27,Findings,Perm,,FT,
Timing,FT,VISITNUM,Visit Number,Num,VISITNUM,"Clinical encounter number. Numeric version of VISIT, used for sorting.",28,Findings,Exp,,,
Timing,FT,VISIT,Visit Name,Char,VISIT,Protocol-defined description of a clinical encounter.,29,Findings,Perm,,,
Timing,FT,VISITDY,Planned Study Day of Visit,Num,VISITDY,Planned study day of VISIT based upon RFSTDTC in Demographics. Should be an integer.,30,Findings,Perm,,,
Timing,FT,TAETORD,Planned Order of Element within Arm,Num,TAETORD,Number that gives the planned order of the Element within the Arm for the element in which the assessment was made.,31,Findings,Perm,,,
Timing,FT,EPOCH,Epoch,Char,EPOCH,Epoch associated with the observation date/time of the functional tests finding.,32,Findings,Perm,(EPOCH),,
Timing,FT,FTDTC,Date/Time of Test,Char,DTC,Collection date and time of functional test.,33,Findings,Exp,ISO 8601,FT,
Timing,FT,FTDY,Study Day of Test,Num,DY,Actual study day of test expressed in integer days relative to the sponsor-defined RFSTDTC in Demographics.,34,Findings,Perm,,FT,
Timing,FT,FTTPT,Planned Time Point Name,Char,TPT,"Text description of time when a measurement or observation should be taken, as defined in the protocol. This may be represented as an elapsed time relative to a fixed reference point, such as time of last dose. See FTTPTNUM and FTTPTREF.",35,Findings,Perm,,FT,
Timing,FT,FTTPTNUM,Planned Time Point Number,Num,TPTNUM,Numeric version of planned time point used in sorting.,36,Findings,Perm,,FT,
Timing,FT,FTELTM,Planned Elapsed Time from Time Point Ref,Char,ELTM,"Planned elapsed time relative to a planned fixed reference (FTTPTREF). Not a clock time or a date/time variable, but an interval, represented as ISO duration.",37,Findings,Perm,ISO 8601,FT,
Timing,FT,FTTPTREF,Time Point Reference,Char,TPTREF,"Description of the fixed reference point referred to by FTELTM, FTTPTNUM, and FTTPT. Examples: ""PREVIOUS DOSE"", ""PREVIOUS MEAL"".",38,Findings,Perm,,FT,
Timing,FT,FTRFTDTC,Date/Time of Reference Time Point,Char,RFTDTC,Date/time for a fixed reference time point defined by FTTPTREF.,39,Findings,Perm,ISO 8601,FT,
Identifier,IE,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Findings,Req,,,
Identifier,IE,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Findings,Req,IE,,
Identifier,IE,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product.,3,Findings,Req,,,
Identifier,IE,IESEQ,Sequence Number,Num,SEQ,Sequence number given to ensure uniqueness of subject records within a domain. May be any valid number.,4,Findings,Req,,IE,
Identifier,IE,IESPID,Sponsor-Defined Identifier,Char,SPID,Sponsor-defined reference number. Perhaps preprinted on the CRF as an explicit line identifier or defined in the sponsor's operational database. Example: Inclusion or Exclusion criteria number from CRF.,5,Findings,Perm,,IE,
Topic,IE,IETESTCD,Inclusion/Exclusion Criterion Short Name,Char,TESTCD,"Short name of the criterion described in IETEST. The value in IETESTCD cannot be longer than 8 characters, nor can it start with a number (e.g., &quot;1TEST&quot; is not valid). IETESTCD cannot contain characters other than letters, numbers, or underscores. Examples: &quot;IN01&quot;, &quot;EX01&quot;.",6,Findings,Req,,IE,
Synonym Qualifier,IE,IETEST,Inclusion/Exclusion Criterion,Char,TEST,Verbatim description of the inclusion or exclusion criterion that was the exception for the subject within the study. IETEST cannot be longer than 200 characters.,7,Findings,Req,,IE,
Grouping Qualifier,IE,IECAT,Inclusion/Exclusion Category,Char,CAT,Used to define a category of related records across subjects.,8,Findings,Req,(IECAT),IE,
Grouping Qualifier,IE,IESCAT,Inclusion/Exclusion Subcategory,Char,SCAT,"A further categorization of the exception criterion. Can be used to distinguish criteria for a sub-study or for to categorize as a major or minor exceptions. Examples: &quot;MAJOR&quot;, &quot;MINOR&quot;.",9,Findings,Perm,,IE,
Result Qualifier,IE,IEORRES,I/E Criterion Original Result,Char,ORRES,"Original response to Inclusion/Exclusion Criterion question, i.e., whether the inclusion or exclusion criterion was met.",10,Findings,Req,(NY),IE,
Result Qualifier,IE,IESTRESC,I/E Criterion Result in Std Format,Char,STRESC,Response to Inclusion/Exclusion criterion result in standard format.,11,Findings,Req,(NY),IE,
Timing,IE,VISITNUM,Visit Number,Num,VISITNUM,"1. Clinical encounter number. \n 2. Numeric version of VISIT, used for sorting.",12,Findings,Perm,,,
Timing,IE,VISIT,Visit Name,Char,VISIT,Protocol-defined description of clinical encounter.May be used in addition to VISITNUM and/or VISITDY.,13,Findings,Perm,,,
Timing,IE,VISITDY,Planned Study Day of Visit,Num,VISITDY,Planned study day of the visit based upon RFSTDTC in Demographics.,14,Findings,Perm,,,
Timing,IE,TAETORD,Planned Order of Element within Arm,Num,TAETORD,Number that gives the planned order of the Element within the Arm for the Element in which the assessment was made.,15,Findings,Perm,,,
Timing,IE,EPOCH,Epoch,Char,EPOCH,Epoch associated with the observation date/time of the inclusion/exclusion finding.,16,Findings,Perm,(EPOCH),,
Timing,IE,IEDTC,Date/Time of Collection,Char,DTC,Collection date and time of the inclusion/exclusion criterion represented in ISO 8601 character format.,17,Findings,Perm,ISO 8601,IE,
Timing,IE,IEDY,Study Day of Collection,Num,DY,"Study day of collection of the inclusion/exclusion exceptions, measured as integer days.Algorithm for calculations must be relative to the sponsor-defined RFSTDTC variable in Demographics. This formula should be consistent across the submission.",18,Findings,Perm,,IE,
Identifier,IS,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Findings,Req,,,
Identifier,IS,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Findings,Req,IS,,
Identifier,IS,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product.,3,Findings,Req,,,
Identifier,IS,ISSEQ,Sequence Number,Num,SEQ,Sequence number given to ensure uniqueness of subject records within a domain. May be any valid number.,4,Findings,Req,,IS,
Identifier,IS,ISGRPID,Group ID,Char,GRPID,Used to tie together a block of related records in a single domain for a subject.,5,Findings,Perm,,IS,
Identifier,IS,ISREFID,Reference ID,Char,REFID,Internal or external specimen identifier. Example: &quot;458975-01&quot;.,6,Findings,Perm,,IS,
Identifier,IS,ISSPID,Sponsor-Defined Identifier,Char,SPID,Sponsor-defined identifier.,7,Findings,Perm,,IS,
Topic,IS,ISTESTCD,Immunogenicity Test/Exam Short Name,Char,TESTCD,"Short name of the measurement, test, or examination described in ISTEST. It can be used as a column name when converting a dataset from a vertical to a horizontal format. The value in ISTESTCD cannot be longer than 8 characters, nor can it start with a number (e.g., &quot;1TEST&quot; is not valid). ISTESTCD cannot contain characters other than letters, numbers, or underscores.",8,Findings,Req,(ISTESTCD),IS,
Synonym Qualifier,IS,ISTEST,Immunogenicity Test or Examination Name,Char,TEST,Verbatim name of the test or examination used to obtain the measurement or finding. The value in ISTEST cannot be longer than 40 characters. Example: &quot;Immunoglobulin E&quot;.,9,Findings,Req,(ISTEST),IS,
Synonym Qualifier,IS,ISCAT,Category for Immunogenicity Test,Char,CAT,Used to define a category of Topic-variable values across subjects. Example: &quot;SEROLOGY&quot;.,10,Findings,Perm,,IS,
Grouping Qualifier,IS,ISSCAT,Subcategory for Immunogenicity Test,Char,SCAT,A further categorization of ISCAT.,11,Findings,Perm,,IS,
Result Qualifier,IS,ISORRES,Results or Findings in Original Units,Char,ORRES,Result of measurement or finding as originally received or collected.,12,Findings,Exp,,IS,
Variable Qualifier,IS,ISORRESU,Original Units,Char,ORRESU,"Original units in which the data were collected. The unit for ISORRES. Examples: &quot;Index Value&quot;, &quot;gpELISA&quot;, &quot;unit/mL&quot;.",13,Findings,Exp,(UNIT),IS,
Result Qualifier,IS,ISSTRESC,Character Result/Finding in Std Format,Char,STRESC,"Contains the result value for all findings, copied or derived from ISORRES, in a standard format or in standard units. ISSTRESC should store all results or findings in character format; if results are numeric, they should also be stored in numeric format in ISSTRESN.",14,Findings,Exp,,IS,
Result Qualifier,IS,ISSTRESN,Numeric Results/Findings in Std. Units,Num,STRESN,Used for continuous or numeric results or findings in standard format; copied in numeric format from ISSTRESC. ISSTRESN should store all numeric test results or findings.,15,Findings,Exp,,IS,
Variable Qualifier,IS,ISSTRESU,Standard Units,Char,STRESU,"Standardized units used for ISSTRESC and ISSTRESN. Examples: &quot;Index Value&quot;, &quot;gpELISA&quot;, &quot;unit/mL&quot;.",16,Findings,Exp,(UNIT),IS,
Record Qualifier,IS,ISSTAT,Completion Status,Char,STAT,Used to indicate a test was not done. Should be null if a result exists in ISORRES.,17,Findings,Perm,(ND),IS,
Record Qualifier,IS,ISREASND,Reason Not Done,Char,REASND,Describes why a measurement or test was not performed. Used in conjunction with ISSTAT when value is &quot;NOT DONE&quot;.,18,Findings,Perm,,IS,
Record Qualifier,IS,ISNAM,Vendor Name,Char,NAM,Name or identifier of the laboratory or vendor who provided the test results.,19,Findings,Perm,,IS,
Record Qualifier,IS,ISSPEC,Specimen Type,Char,SPEC,Defines the types of specimen used for a measurement. Example: &quot;SERUM&quot;.,20,Findings,Perm,(SPECTYPE),IS,
Record Qualifier,IS,ISMETHOD,Method of Test or Examination,Char,METHOD,"Method of the test or examination. Examples: &quot;ELISA&quot;, &quot;ELISPOT&quot;.",21,Findings,Perm,(METHOD),IS,
Record Qualifier,IS,ISLOBXFL,Last Observation Before Exposure Flag,Char,LOBXFL,Operationally-derived indicator used to identify the last non-missing value prior to RFXSTDTC. The value should be &quot;Y&quot; or null.,22,Findings,Perm,(NY),IS,
Record Qualifier,IS,ISBLFL,Baseline Flag,Char,BLFL,Indicator used to identify a baseline value. Should be &quot;Y&quot; or null. Note that ISBLFL is retained for backward compatibility. The authoritative baseline for statistical analysis is in an ADaM dataset.,23,Findings,Perm,(NY),IS,
Variable Qualifier,IS,ISLLOQ,Lower Limit of Quantitation,Num,LLOQ,Indicates the lower limit of quantitation for an assay. Units will be those used for ISSTRESU.,24,Findings,Exp,,IS,
Timing,IS,VISITNUM,Visit Number,Num,VISITNUM,"1. Clinical encounter number. \n 2. Numeric version of VISIT, used for sorting.",25,Findings,Exp,,,
Timing,IS,VISIT,Visit Name,Char,VISIT,Protocol-defined description of a clinical encounter.May be used in addition to VISITNUM and/or VISITDY.,26,Findings,Perm,,,
Timing,IS,VISITDY,Planned Study Day of Visit,Num,VISITDY,Planned study day of the visit based upon RFSTDTC in Demographics.,27,Findings,Perm,,,
Timing,IS,TAETORD,Planned Order of Element within Arm,Num,TAETORD,Number that gives the planned order of the Element within the Arm.,28,Findings,Perm,,,
Timing,IS,EPOCH,Epoch,Char,EPOCH,"Epoch associated with the start date/time of the observation, or the date/time of collection if start date/time is not collected.",29,Findings,Perm,(EPOCH),,
Timing,IS,ISDTC,Date/Time of Collection,Char,DTC,Collection date and time of an observation represented in ISO 8601.,30,Findings,Exp,ISO 8601,IS,
Timing,IS,ISDY,Study Day of Visit/Collection/Exam,Num,DY,Actual study day of visit/collection/exam expressed in integer days relative to sponsor-defined RFSTDTC in Demographics.,31,Findings,Perm,,IS,
Identifier,LB,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Findings,Req,,,
Identifier,LB,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Findings,Req,LB,,
Identifier,LB,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product.,3,Findings,Req,,,
Identifier,LB,LBSEQ,Sequence Number,Num,SEQ,Sequence number given to ensure uniqueness of subject records within a domain. May be any valid number.,4,Findings,Req,,LB,
Identifier,LB,LBGRPID,Group ID,Char,GRPID,Used to tie together a block of related records in a single domain for a subject.,5,Findings,Perm,,LB,
Identifier,LB,LBREFID,Specimen ID,Char,REFID,Internal or external specimen identifier. Example: Specimen ID.,6,Findings,Perm,,LB,
Identifier,LB,LBSPID,Sponsor-Defined Identifier,Char,SPID,Sponsor-defined reference number. Perhaps preprinted on the CRF as an explicit line identifier or defined in the sponsor's operational database. Example: Line number on the Lab page.,7,Findings,Perm,,LB,
Topic,LB,LBTESTCD,Lab Test or Examination Short Name.,Char,TESTCD,"Short name of the measurement, test, or examination described in LBTEST. It can be used as a column name when converting a dataset from a vertical to a horizontal format. The value in LBTESTCD cannot be longer than 8 characters, nor can it start with a number (e.g., &quot;1TEST&quot; is not valid). LBTESTCD cannot contain characters other than letters, numbers, or underscores. Examples: &quot;ALT&quot;, &quot;LDH&quot;.",8,Findings,Req,(LBTESTCD),LB,
Synonym Qualifier,LB,LBTEST,Lab Test or Examination Name,Char,TEST,"Verbatim name of the test or examination used to obtain the measurement or finding. Note any test normally performed by a clinical laboratory is considered a lab test. The value in LBTEST cannot be longer than 40 characters. Examples: &quot;Alanine Aminotransferase&quot;, &quot;Lactate Dehydrogenase&quot;.",9,Findings,Req,(LBTEST),LB,
Grouping Qualifier,LB,LBCAT,Category for Lab Test,Char,CAT,"Used to define a category of related records across subjects. Examples: &quot;HEMATOLOGY&quot;, &quot;URINALYSIS&quot;, &quot;CHEMISTRY&quot;.",10,Findings,Exp,,LB,
Grouping Qualifier,LB,LBSCAT,Subcategory for Lab Test,Char,SCAT,"A further categorization of a test category such as &quot;DIFFERENTIAL&quot;, &quot;COAGULATION&quot;, &quot;LIVER FUNCTION&quot;, &quot;ELECTROLYTES&quot;.",11,Findings,Perm,,LB,
Result Qualifier,LB,LBORRES,Result or Finding in Original Units,Char,ORRES,Result of the measurement or finding as originally received or collected.,12,Findings,Exp,,LB,
Variable Qualifier,LB,LBORRESU,Original Units,Char,ORRESU,Original units in which the data were collected. The unit for LBORRES. Example: &quot;g/L&quot;.,13,Findings,Exp,(UNIT),LB,
Variable Qualifier,LB,LBORNRLO,Reference Range Lower Limit in Orig Unit,Char,ORNRLO,Lower end of reference range for continuous measurement in original units. Should be populated only for continuous results.,14,Findings,Exp,,LB,
Variable Qualifier,LB,LBORNRHI,Reference Range Upper Limit in Orig Unit,Char,ORNRHI,Upper end of reference range for continuous measurement in original units. Should be populated only for continuous results.,15,Findings,Exp,,LB,
Result Qualifier,LB,LBSTRESC,Character Result/Finding in Std Format,Char,STRESC,"Contains the result value for all findings, copied or derived from LBORRES in a standard format or standard units. LBSTRESC should store all results or findings in character format; if results are numeric, they should also be stored in numeric format in LBSTRESN. For example, if a test has results &quot;NONE&quot;, &quot;NEG&quot;, and &quot;NEGATIVE&quot; in LBORRES and these results effectively have the same meaning, they could be represented in standard format in LBSTRESC as &quot;NEGATIVE&quot;. For other examples, see general assumptions.",16,Findings,Exp,(LBSTRESC),LB,
Result Qualifier,LB,LBSTRESN,Numeric Result/Finding in Standard Units,Num,STRESN,Used for continuous or numeric results or findings in standard format; copied in numeric format from LBSTRESC. LBSTRESN should store all numeric test results or findings.,17,Findings,Exp,,LB,
Variable Qualifier,LB,LBSTRESU,Standard Units,Char,STRESU,Standardized unit used for LBSTRESC or LBSTRESN.,18,Findings,Exp,(UNIT),LB,
Variable Qualifier,LB,LBSTNRLO,Reference Range Lower Limit-Std Units,Num,STNRLO,Lower end of reference range for continuous measurements for LBSTRESC/LBSTRESN in standardized units. Should be populated only for continuous results.,19,Findings,Exp,,LB,
Variable Qualifier,LB,LBSTNRHI,Reference Range Upper Limit-Std Units,Num,STNRHI,Upper end of reference range for continuous measurements in standardized units. Should be populated only for continuous results.,20,Findings,Exp,,LB,
Variable Qualifier,LB,LBSTNRC,Reference Range for Char Rslt-Std Units,Char,STNRC,"For normal range values that are character in ordinal scale or if categorical ranges were supplied (e.g., &quot;-1 to +1&quot;, &quot;NEGATIVE TO TRACE&quot;).",21,Findings,Perm,,LB,
Variable Qualifier,LB,LBSTREFC,Reference Result in Standard Format,Char,STREFC,Reference value for the result or finding copied or derived from LBORREF in a standard format.,22,Findings,Exp,,LB,
Variable Qualifier,LB,LBNRIND,Reference Range Indicator,Char,NRIND,"1. Indicates where the value falls with respect to reference range defined by LBORNRLO and LBORNRHI, LBSTNRLO and LBSTNRHI, or by LBSTNRC. Examples: &quot;NORMAL&quot;, &quot;ABNORMAL&quot;, &quot;HIGH&quot;, &quot;LOW&quot;. \n 2. Sponsors should specify in the study metadata (Comments column in the Define-XML document) whether LBNRIND refers to the original or standard reference ranges and results. \n 3. Should not be used to indicate clinical significance.",23,Findings,Exp,(NRIND),LB,
Record Qualifier,LB,LBSTAT,Completion Status,Char,STAT,Used to indicate exam not done. Should be null if a result exists in LBORRES.,24,Findings,Perm,(ND),LB,
Record Qualifier,LB,LBREASND,Reason Test Not Done,Char,REASND,"Describes why a measurement or test was not performed, e.g., &quot;BROKEN EQUIPMENT&quot;, &quot;SUBJECT REFUSED&quot;, or &quot;SPECIMEN LOST&quot;. Used in conjunction with LBSTAT when value is &quot;NOT DONE&quot;.",25,Findings,Perm,,LB,
Record Qualifier,LB,LBNAM,Vendor Name,Char,NAM,The name or identifier of the laboratory that performed the test.,26,Findings,Perm,,LB,
Synonym Qualifier,LB,LBLOINC,LOINC Code,Char,LOINC,Code for the lab test from the LOINC code system.The sponsor is expected to provide the dictionary name and version used to map the terms utilizing the Define-XML external codelist attributes.,27,Findings,Perm,,LB,
Record Qualifier,LB,LBSPEC,Specimen Type,Char,SPEC,"Defines the type of specimen used for a measurement. Examples: &quot;SERUM&quot;, &quot;PLASMA&quot;, &quot;URINE&quot;, &quot;DNA&quot;, &quot;RNA&quot;.",28,Findings,Perm,(SPECTYPE),LB,
Record Qualifier,LB,LBSPCCND,Specimen Condition,Char,SPCCND,"Free or standardized text describing the condition of the specimen, e.g., &quot;HEMOLYZED&quot;, &quot;ICTERIC&quot;, &quot;LIPEMIC&quot;.",29,Findings,Perm,(SPECCOND),LB,
Record Qualifier,LB,LBMETHOD,Method of Test or Examination,Char,METHOD,"Method of the test or examination. Examples: &quot;EIA&quot; (Enzyme Immunoassay), &quot;ELECTROPHORESIS&quot;, &quot;DIPSTICK&quot;.",30,Findings,Perm,(METHOD),LB,
Record Qualifier,LB,LBLOBXFL,Last Observation Before Exposure Flag,Char,LOBXFL,Operationally-derived indicator used to identify the last non-missing value prior to RFXSTDTC. The value should be &quot;Y&quot; or null.,31,Findings,Exp,(NY),LB,
Record Qualifier,LB,LBBLFL,Baseline Flag,Char,BLFL,Indicator used to identify a baseline value. Should be &quot;Y&quot; or null. Note that LBBLFL is retained for backward compatibility. The authoritative baseline for statistical analysis is in an ADaM dataset.,32,Findings,Perm,(NY),LB,
Record Qualifier,LB,LBFAST,Fasting Status,Char,FAST,"Indicator used to identify fasting status such as &quot;Y&quot;, &quot;N&quot;, &quot;U&quot;, or null if not relevant.",33,Findings,Perm,(NY),LB,
Record Qualifier,LB,LBDRVFL,Derived Flag,Char,DRVFL,"Used to indicate a derived record. The value should be &quot;Y&quot; or null. Records that represent the average of other records, or do not come from the CRF, or are not as originally received or collected are examples of records that might be derived for the submission datasets. If LBDRVFL = &quot;Y&quot;, then LBORRES may be null, with LBSTRESC and (if numeric) LBSTRESN having the derived value.",34,Findings,Perm,(NY),LB,
Variable Qualifier,LB,LBTOX,Toxicity,Char,TOX,"Description of toxicity quantified by LBTOXGR. The sponsor is expected to provide the name of the scale and version used to map the terms, utilizing the external codelist element in the Define-XML document.",35,Findings,Perm,,LB,
Record Qualifier,LB,LBTOXGR,Standard Toxicity Grade,Char,TOXGR,"Records toxicity grade value using a standard toxicity scale (such as the NCI CTCAE). If value is from a numeric scale, represent only the number (e.g., &quot;2&quot; and not &quot;Grade 2&quot;). The sponsor is expected to provide the name of the scale and version used to map the terms, utilizing the external codelist element in the Define-XML document.",36,Findings,Perm,,LB,
Timing,LB,VISITNUM,Visit Number,Num,VISITNUM,"Clinical encounter number.Numeric version of VISIT, used for sorting.",37,Findings,Exp,,,
Timing,LB,VISIT,Visit Name,Char,VISIT,Protocol-defined description of clinical encounter.May be used in addition to VISITNUM and/or VISITDY.,38,Findings,Perm,,,
Timing,LB,VISITDY,Planned Study Day of Visit,Num,VISITDY,Planned study day of the visit based upon RFSTDTC in Demographics.,39,Findings,Perm,,,
Timing,LB,TAETORD,Planned Order of Element within Arm,Num,TAETORD,Number that gives the planned order of the Element within the Arm.,40,Findings,Perm,,,
Timing,LB,EPOCH,Epoch,Char,EPOCH,"Epoch associated with the start date/time of the observation, or the date/time of collection if start date/time is not collected.",41,Findings,Perm,(EPOCH),,
Timing,LB,LBDTC,Date/Time of Specimen Collection,Char,DTC,Date/time of specimen collection represented in ISO 8601 character format.,42,Findings,Exp,ISO 8601,LB,
Timing,LB,LBENDTC,End Date/Time of Specimen Collection,Char,ENDTC,End date/time of specimen collection represented in ISO 8601 character format.,43,Findings,Perm,ISO 8601,LB,
Timing,LB,LBDY,Study Day of Specimen Collection,Num,DY,"Study day of specimen collection, measured as integer days.Algorithm for calculations must be relative to the sponsor-defined RFSTDTC variable in Demographics. This formula should be consistent across the submission.",44,Findings,Perm,,LB,
Timing,LB,LBENDY,Study Day of End of Observation,Num,ENDY,Actual study day of end of observation expressed in integer days relative to the sponsor-defined RFSTDTC in Demographics.,45,Findings,Perm,,LB,
Timing,LB,LBTPT,Planned Time Point Name,Char,TPT,"Text description of time when specimen should be taken.This may be represented as an elapsed time relative to a fixed reference point, such as time of last dose. See LBTPTNUM and LBTPTREF. Examples: &quot;Start&quot;, &quot;5 min post&quot;.",46,Findings,Perm,,LB,
Timing,LB,LBTPTNUM,Planned Time Point Number,Num,TPTNUM,Numerical version of LBTPT to aid in sorting.,47,Findings,Perm,,LB,
Timing,LB,LBELTM,Planned Elapsed Time from Time Point Ref,Char,ELTM,"Planned elapsed time (in ISO 8601) relative to a planned fixed reference (LBTPTREF). This variable is useful where there are repetitive measures. Not a clock time or a date/time variable. Represented as ISO 8601 duration. Examples: &quot;-PT15M&quot; to represent the period of 15 minutes prior to the reference point indicated by LBTPTREF, or &quot;PT8H&quot; to represent the period of 8 hours after the reference point indicated by LBTPTREF.",48,Findings,Perm,ISO 8601,LB,
Timing,LB,LBTPTREF,Time Point Reference,Char,TPTREF,"Name of the fixed reference point referred to by LBELTM, LBTPTNUM, and LBTPT. Examples: PREVIOUS DOSE, PREVIOUS MEAL.",49,Findings,Perm,,LB,
Timing,LB,LBRFTDTC,Date/Time of Reference Time Point,Char,RFTDTC,"Date/time of the reference time point, LBTPTREF.",50,Findings,Perm,ISO 8601,LB,
Identifier,MB,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Findings,Req,,,
Identifier,MB,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Findings,Req,MB,,
Identifier,MB,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product.,3,Findings,Req,,,
Identifier,MB,FOCID,Focus of Study-Specific Interest,Char,FOCID,"Identification of a focus of study-specific interest on or within a subject or specimen as called out in the protocol for which a measurement, test, or examination was performed.The value in this variable should have inherent semantic meaning.",4,Findings,Perm,,,
Identifier,MB,MBSEQ,Sequence Number,Num,SEQ,Sequence number to ensure uniqueness of records within a dataset for a subject. May be any valid number.,5,Findings,Req,,MB,
Identifier,MB,MBGRPID,Group ID,Char,GRPID,"Optional group identifier, used to link together a block of related records within a subject in a domain. In SDTMIG v3.2, this was an Expected variable. In this version, the core designation has been changed to Permissible.",6,Findings,Perm,,MB,
Identifier,MB,MBREFID,Reference ID,Char,REFID,Internal or external specimen identifier such as the sample ID for a subject sample from which a microbial culture was generated.,7,Findings,Perm,,MB,
Identifier,MB,MBSPID,Sponsor-Defined Identifier,Char,SPID,Sponsor-defined reference number. Perhaps preprinted on the CRF as an explicit line identifier or defined in the sponsor's operational database.,8,Findings,Perm,,MB,
Identifier,MB,MBLNKID,Link ID,Char,LNKID,"Identifier used to link related records across domains. This may be a one-to-one or a one-to-many relationship. For example, it may be used to link genetic findings (in the PF domain) about a microbe to the original culture of that microbe (in MB), or to susceptibility records (in MS) if needed.",9,Findings,Perm,,MB,
Identifier,MB,MBLNKGRP,Link Group ID,Char,LNKGRP,Identifier used to link related records across domains. This will usually be a many-to-one relationship.,10,Findings,Perm,,MB,
Topic,MB,MBTESTCD,Microbiology Test or Finding Short Name,Char,TESTCD,"Short name of the measurement, test, or finding described in MBTEST. It can be used as a column name when converting a dataset from a vertical to a horizontal format. The value in MBTESTCD cannot be longer than 8 characters, nor can it start with a number (e.g., &quot;1TEST&quot; is not valid). MBTESTCD cannot contain characters other than letters, numbers, or underscores. Example: &quot;MCORGIDN&quot; for Microbial Organism Identification; &quot;GMNCOC&quot; for Gram Negative Cocci.",11,Findings,Req,(MBTESTCD),MB,
Synonym Qualifier,MB,MBTEST,Microbiology Test or Finding Name,Char,TEST,Verbatim name of the test or examination used to obtain the measurement or finding. The value in MBTEST cannot be longer than 40 characters. Examples:&quot;Microbial Organism Identification; &quot;Gram Negative Cocci&quot;; &quot;HIV-1 RNA&quot;.,12,Findings,Req,(MBTEST),MB,
Variable Qualifier,MB,MBTSTDTL,"Measurement, Test or Examination Detail",Char,TSTDTL,"Further description of MBTESTCD and MBTEST. Example: &quot;VIRAL LOAD&quot; (when MBTESTCD represents viral genetic material, such as &quot;HCRNA&quot;); &quot;QUANTIFICATION&quot; when MBTESTCD represents any organism being quantified.",13,Findings,Perm,,MB,
Grouping Qualifier,MB,MBCAT,Category,Char,CAT,Used to define a category of related records.,14,Findings,Perm,,MB,
Grouping Qualifier,MB,MBSCAT,Subcategory,Char,SCAT,Used to define a further categorization of MBCAT values.,15,Findings,Perm,,MB,
Result Qualifier,MB,MBORRES,Result or Finding in Original Units,Char,ORRES,"Result of the Microbiology measurement or finding as originally received or collected. Examples for &quot;GRAM STAIN&quot; findings: &quot;+3 MODERATE&quot;, &quot;+2 FEW&quot;, &quot;<10&quot;. Examples for &quot;CULTURE PLATE&quot; findings: &quot;KLEBSIELLA PNEUMONIAE&quot;, &quot;STREPTOCOCCUS PNEUMONIAE&quot;.",16,Findings,Exp,,MB,
Variable Qualifier,MB,MBORRESU,Original Units,Char,ORRESU,Original unit for MBORRES. Example: &quot;mcg/mL&quot;.,17,Findings,Perm,(UNIT),MB,
Result Qualifier,MB,MBSTRESC,Result or Finding in Standard Format,Char,STRESC,"Contains the result value for all findings, copied or derived from MBORRES in a standard format or standard units. MBSTRESC should store all results or findings in character format; if results are numeric, they should also be stored in numeric format in MBSTRESN. For example, if a test has results &quot;+3 MODERATE&quot;, &quot;MOD&quot;, and &quot;MODERATE&quot; in MBORRES and these results effectively have the same meaning, they could be represented in standard format in MBSTRESC as &quot;MODERATE&quot;.",18,Findings,Exp,,MB,
Result Qualifier,MB,MBSTRESN,Numeric Result/Finding in Standard Units,Num,STRESN,Used for continuous or numeric results or findings in standard format; copied in numeric format from MBSTRESC. MBSTRESN should store all numeric test results or findings.,19,Findings,Perm,,MB,
Variable Qualifier,MB,MBSTRESU,Standard Units,Char,STRESU,Standardized units used for MBSTRESC and MBSTRESN.,20,Findings,Perm,(UNIT),MB,
Variable Qualifier,MB,MBRESCAT,Result Category,Char,RESCAT,"Used to categorize the result of a finding in a standard format. In SDTMIG v3.2, this was an Expected variable. In this version, the core designation has been changed to Permissible.",21,Findings,Perm,,MB,
Record Qualifier,MB,MBSTAT,Completion Status,Char,STAT,"Used to indicate that a question was not asked or a test was not done, or that a test was attempted but did not generate a result. Should be null or have a value of &quot;NOT DONE&quot;.",22,Findings,Perm,(ND),MB,
Record Qualifier,MB,MBREASND,Reason Not Done,Char,REASND,Reason not done. Used in conjunction with MBSTAT when value is NOT DONE. Examples: &quot;BROKEN EQUIPMENT&quot; or &quot;SUBJECT REFUSED&quot;.,23,Findings,Perm,,MB,
Record Qualifier,MB,MBNAM,Laboratory/Vendor Name,Char,NAM,"Name or identifier of the vendor (e.g., laboratory) that provided the test results.",24,Findings,Perm,,MB,
Synonym Qualifier,MB,MBLOINC,LOINC Code,Char,LOINC,"Logical Observation Identifiers Names and Codes (LOINC) code for the topic variable, such as a lab test.",25,Findings,Perm,,MB,
Record Qualifier,MB,MBSPEC,Specimen Material Type,Char,SPEC,"Defines the type of specimen used for a measurement. Examples: &quot;SPUTUM&quot;, &quot;BLOOD&quot;, &quot;PUS&quot;.",26,Findings,Perm,(SPECTYPE),MB,
Record Qualifier,MB,MBSPCCND,Specimen Condition,Char,SPCCND,Free or standardized text describing the condition of the specimen. Example: &quot;CONTAMINATED&quot;.,27,Findings,Perm,(SPECCOND),MB,
Record Qualifier,MB,MBLOC,Specimen Collection Location,Char,LOC,Anatomical location relevant to the collection of the measurement.,28,Findings,Perm,(LOC),MB,
Variable Qualifier,MB,MBLAT,Laterality,Char,LAT,"Qualifier for specimen collection location further detailing laterality. Examples: &quot;RIGHT&quot;, &quot;LEFT&quot;, &quot;BILATERAL&quot;.",29,Findings,Perm,(LAT),MB,
Variable Qualifier,MB,MBDIR,Directionality,Char,DIR,"Qualifier for specimen collection location further detailing directionality. Examples: &quot;ANTERIOR&quot;, &quot;LOWER&quot;, &quot;PROXIMAL&quot;.",30,Findings,Perm,(DIR),MB,
Record Qualifier,MB,MBMETHOD,Method of Test or Examination,Char,METHOD,"Method of the test or examination. Example: &quot;GRAM STAIN&quot;,&quot;MICROBIAL CULTURE, LIQUID&quot;, &quot;QUANTITATIVE REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION&quot;.",31,Findings,Exp,(METHOD),MB,
Record Qualifier,MB,MBLOBXFL,Last Observation Before Exposure Flag,Char,LOBXFL,Operationally-derived indicator used to identify the last non-missing value prior to RFXSTDTC. The value should be &quot;Y&quot; or null.,32,Findings,Perm,(NY),MB,
Record Qualifier,MB,MBBLFL,Baseline Flag,Char,BLFL,Indicator used to identify a baseline value. Should be &quot;Y&quot; or null. Note that MBBLFL is retained for backward compatibility. The authoritative baseline for statistical analysis is in an ADaM dataset.,33,Findings,Perm,(NY),MB,
Record Qualifier,MB,MBFAST,Fasting Status,Char,FAST,"Indicator used to identify fasting status. Valid values include &quot;Y&quot;, &quot;N&quot;, &quot;U&quot; or null if not relevant.",34,Findings,Perm,(NY),MB,
Record Qualifier,MB,MBDRVFL,Derived Flag,Char,DRVFL,"Used to indicate a derived record (e.g., a record that represents the average of other records such as a computed baseline). Should be &quot;Y&quot; or null.",35,Findings,Perm,(NY),MB,
Timing,MB,VISITNUM,Visit Number,Num,VISITNUM,"Clinical encounter number. Numeric version of VISIT, used for sorting.",36,Findings,Exp,,,
Timing,MB,VISIT,Visit Name,Char,VISIT,Protocol-defined description of a clinical encounter.,37,Findings,Perm,,,
Timing,MB,VISITDY,Planned Study Day of Visit,Num,VISITDY,Planned study day of VISIT. Should be an integer.,38,Findings,Perm,,,
Timing,MB,TAETORD,Planned Order of Element within Arm,Num,TAETORD,Number that gives the planned order of the Element within the Arm for the Element which the specimen collection occurred.,39,Findings,Perm,,,
Timing,MB,EPOCH,Epoch,Char,EPOCH,Epoch associated with the date/time at which the specimen was collected.,40,Findings,Perm,(EPOCH),,
Timing,MB,MBDTC,Date/Time of Collection,Char,DTC,Date/time of specimen collection.,41,Findings,Exp,ISO 8601,MB,
Timing,MB,MBDY,Study Day of Visit/Collection/Exam,Num,DY,"1. Study day of the specimen collection, measured as integer days. \n 2. Algorithm for calculations must be relative to the sponsor-defined RFSTDTC variable in Demographics. This formula should be consistent across the submission.",42,Findings,Perm,,MB,
Timing,MB,MBTPT,Planned Time Point Name,Char,TPT,"Text description of time when specimen should be taken.This may be represented as an elapsed time relative to a fixed reference point, such as time of last dose. See MBTPTNUM and MBTPTREF. Examples: &quot;Start&quot;, &quot;5 min post&quot;.",43,Findings,Perm,,MB,
Timing,MB,MBTPTNUM,Planned Time Point Number,Num,TPTNUM,Numeric version of MBTPT used in sorting.,44,Findings,Perm,,MB,
Timing,MB,MBELTM,Planned Elapsed Time from Time Point Ref,Char,ELTM,"Planned elapsed time (in ISO 8601) relative to a planned fixed reference (MBTPTREF). This variable is useful where there are repetitive measures. Not a clock time or a date time variable. Represented as an ISO 8601 duration. Examples: &quot;-PT15M&quot; to represent the period of 15 minutes prior to the reference point indicated by MBTPTREF, or &quot;PT8H&quot; to represent the period of 8 hours after the reference point indicated by MBTPTREF.",45,Findings,Perm,ISO 8601,MB,
Timing,MB,MBTPTREF,Time Point Reference,Char,TPTREF,"Name of the fixed reference point referred to by MBELTM, MBTPTNUM, and MBTPT. Example: &quot;PREVIOUS DOSE&quot;.",46,Findings,Perm,,MB,
Timing,MB,MBRFTDTC,Date/Time of Reference Time Point,Char,RFTDTC,"Date/time for a fixed reference time point, MBTPTREF.",47,Findings,Perm,ISO 8601,MB,
Identifier,MI,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Findings,Req,,,
Identifier,MI,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Findings,Req,MI,,
Identifier,MI,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product.,3,Findings,Req,,,
Identifier,MI,MISEQ,Sequence Number,Num,SEQ,Sequence number given to ensure uniqueness of subject records within a domain. May be any valid number.,4,Findings,Req,,MI,
Identifier,MI,MIGRPID,Group ID,Char,GRPID,Used to tie together a block of related records in a single domain for a subject. This is not the treatment group number.,5,Findings,Perm,,MI,
Identifier,MI,MIREFID,Reference ID,Char,REFID,Internal or external specimen identifier. Example: Specimen barcode number.,6,Findings,Perm,,MI,
Identifier,MI,MISPID,Sponsor-Defined Identifier,Char,SPID,Sponsor-defined reference number. Perhaps preprinted on the CRF as an explicit line identifier or defined in the sponsor's operational database. Example: Line number from the MI Findings page.,7,Findings,Perm,,MI,
Topic,MI,MITESTCD,Microscopic Examination Short Name,Char,TESTCD,"Short name of the measurement, test, or examination described in MITEST. It can be used as a column name when converting a dataset from a vertical to a horizontal format. The value in MITESTCD cannot be longer than 8 characters, nor can it start with a number (e.g., ""1TEST"" is not valid). MITESTCD cannot contain characters other than letters, numbers, or underscores. Examples: ""HER2"", ""BRCA1"",""TTF1"".",8,Findings,Req,(MITSCD),MI,
Synonym Qualifier,MI,MITEST,Microscopic Examination Name,Char,TEST,"Verbatim name of the test or examination used to obtain the measurement or finding. The value in MITEST cannot be longer than 40 characters. Examples: ""Human Epidermal Growth Factor Receptor 2"", ""Breast Cancer Susceptibility Gene 1"", ""Thyroid Transcription Factor 1"".",9,Findings,Req,(MITS),MI,
Record Qualifier,MI,MITSTDTL,Microscopic Examination Detail,Char,TSTDTL,"Further description of the test performed in producing the MI result. This would be used to represent specific attributes, such as intensity score or percentage of cells displaying presence of the biomarker or compound.",10,Findings,Perm,(MIFTSDTL),MI,
Grouping Qualifier,MI,MICAT,Category for Microscopic Finding,Char,CAT,Used to define a category of related records.,11,Findings,Perm,,MI,
Grouping Qualifier,MI,MISCAT,Subcategory for Microscopic Finding,Char,SCAT,Used to define a further categorization of MICAT.,12,Findings,Perm,,MI,
Result Qualifier,MI,MIORRES,Result or Finding in Original Units,Char,ORRES,Result of the histopathology measurement or finding as originally received or collected.,13,Findings,Exp,,MI,
Variable Qualifier,MI,MIORRESU,Original Units,Char,ORRESU,Original unit for MIORRES.,14,Findings,Perm,(UNIT),MI,
Result Qualifier,MI,MISTRESC,Character Result/Finding in Std Format,Char,STRESC,"Contains the result value for all findings, copied or derived from MIORRES in a standard format or standard units. MISTRESC should store all results or findings in character format; if results are numeric, they should also be stored in numeric format in MISTRESN.",15,Findings,Exp,,MI,
Result Qualifier,MI,MISTRESN,Numeric Result/Finding in Standard Units,Num,STRESN,Used for continuous or numeric results or findings in standard format; copied in numeric format from MISTRESC. MISTRESN should store all numeric test results or findings.,16,Findings,Perm,,MI,
Variable Qualifier,MI,MISTRESU,Standard Units,Char,STRESU,Standardized unit used for MISTRESC and MISTRESN.,17,Findings,Perm,(UNIT),MI,
Variable Qualifier,MI,MIRESCAT,Result Category,Char,RESCAT,Used to categorize the result of a finding. Examples: "MALIGNANT" or "BENIGN" for tumor findings.,18,Findings,Perm,,MI,
Record Qualifier,MI,MISTAT,Completion Status,Char,STAT,Used to indicate examination not done or result is missing. Should be null if a result exists in MIORRES or have a value of "NOT DONE" when MIORRES = "NULL".,19,Findings,Perm,(ND),MI,
Record Qualifier,MI,MIREASND,Reason Not Done,Char,REASND,"Reason not done. Used in conjunction with MISTAT when value is NOT DONE. Examples: ""SAMPLE AUTOLYZED"", ""SPECIMEN LOST"".",20,Findings,Perm,,MI,
Record Qualifier,MI,MINAM,Laboratory/Vendor Name,Char,NAM,"Name or identifier of the vendor (e.g., laboratory) that provided the test results.",21,Findings,Perm,,MI,
Record Qualifier,MI,MISPEC,Specimen Material Type,Char,SPEC,"Subject of the observation. Defines the type of specimen used for a measurement. Examples: ""TISSUE"", ""BLOOD"", ""BONE MARROW"".",22,Findings,Req,(SPECTYPE),MI,
Record Qualifier,MI,MISPCCND,Specimen Condition,Char,SPCCND,Free or standardized text describing the condition of the specimen. Example: "AUTOLYZED".,23,Findings,Exp,(SPECCOND),MI,
Record Qualifier,MI,MILOC,Specimen Collection Location,Char,LOC,"Location relevant to the collection of the specimen. Examples: ""LUNG"", ""KNEE JOINT"", ""ARM"", ""THIGH"".",24,Findings,Perm,(LOC),MI,
Variable Qualifier,MI,MILAT,Specimen Laterality within Subject,Char,LAT,"Qualifier for laterality of the location of the specimen in MILOC. Examples: ""LEFT"", ""RIGHT"", ""BILATERAL"".",25,Findings,Perm,(LAT),MI,
Variable Qualifier,MI,MIDIR,Specimen Directionality within Subject,Char,DIR,"Qualifier for directionality of the location of the specimen in MILOC. Examples: ""DORSAL"", ""PROXIMAL"".",26,Findings,Perm,(DIR),MI,
Record Qualifier,MI,MIMETHOD,Method of Test or Examination,Char,METHOD,"Method of the test or examination. This could include the technique or type of staining used for the slides. Examples: ""IHC"", ""Crystal Violet"", ""Safranin"", ""Trypan Blue"", or ""Propidium Iodide"".",27,Findings,Perm,(METHOD),MI,
Record Qualifier,MI,MILOBXFL,Last Observation Before Exposure Flag,Char,LOBXFL,Operationally-derived indicator used to identify the last non-missing value prior to RFXSTDTC. The value should be "Y" or null.,28,Findings,Perm,(NY),MI,
Record Qualifier,MI,MIBLFL,Baseline Flag,Char,BLFL,Indicator used to identify a baseline value. The value should be "Y" or null. Note that MIBLFL is retained for backward compatibility. The authoritative baseline flag for statistical analysis is in an ADaM dataset.,29,Findings,Exp,(NY),MI,
Record Qualifier,MI,MIEVAL,Evaluator,Char,EVAL,"Role of the person who provided the evaluation. Example: ""PATHOLOGIST"", ""PEER REVIEW"", ""SPONSOR PATHOLOGIST"".",30,Findings,Perm,(EVAL),MI,
Timing,MI,VISITNUM,Visit Number,Num,VISITNUM,"1. Clinical encounter number. \n 2. Numeric version of VISIT, used for sorting.",31,Findings,Exp,,,
Timing,MI,VISIT,Visit Name,Char,VISIT,1. Protocol-defined description of clinical encounter. \n 2. May be used in addition to VISITNUM and/or VISITDY.,32,Findings,Perm,,,
Timing,MI,VISITDY,Planned Study Day of Visit,Num,VISITDY,Planned study day of the visit based upon RFSTDTC in Demographics.,33,Findings,Perm,,,
Timing,MI,TAETORD,Planned Order of Element within Arm,Num,TAETORD,Number that gives the planned order of the Element within the Arm for the element in which the assessment was made.,34,Findings,Perm,,,
Timing,MI,EPOCH,Epoch,Char,EPOCH,Epoch associated with the date/time at which the specimen was collected.,35,Findings,Perm,(EPOCH),,
Timing,MI,MIDTC,Date/Time of Specimen Collection,Char,DTC,"Date/time of specimen collection, in ISO 8601 format.",36,Findings,Exp,ISO 8601,MI,
Timing,MI,MIDY,Study Day of Specimen Collection,Num,DY,"Study day of specimen collection, in integer days. The algorithm for calculations must be relative to the sponsor-defined RFSTDTC variable in the Demographics (DM) domain.",37,Findings,Perm,,MI,
Identifier,MK,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Findings,Req,,,
Identifier,MK,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Findings,Req,MK,,
Identifier,MK,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product.,3,Findings,Req,,,
Identifier,MK,MKSEQ,Sequence Number,Num,SEQ,"Sequence number to ensure uniqueness of records within a dataset for a subject (or within a parameter, in the case of the Trial Summary domain). May be any valid number (including decimals) and does not have to start at 1.",4,Findings,Req,,MK,
Identifier,MK,MKGRPID,Group ID,Char,GRPID,Used to link together a block of related records within a subject in a domain.,5,Findings,Perm,,MK,
Identifier,MK,MKREFID,Reference ID,Char,REFID,Optional internal or external identifier such as lab specimen ID or a medical image.,6,Findings,Perm,,MK,
Identifier,MK,MKSPID,Sponsor-Defined Identifier,Char,SPID,Sponsor-defined identifier. Example: Preprinted line identifier on a Concomitant Medications page.,7,Findings,Perm,,MK,
Identifier,MK,MKLNKID,Link ID,Char,LNKID,Identifier used to link related records across domains. This may be a one-to-one or a one-to-many relationship.,8,Findings,Perm,,MK,
Identifier,MK,MKLNKGRP,Link Group ID,Char,LNKGRP,Identifier used to link related records across domains. This will usually be a many-to-one relationship.,9,Findings,Perm,,MK,
Topic,MK,MKTESTCD,Short Name of Musculoskeletal Test,Char,TESTCD,"Short character value for MKTEST used as a column name when converting a dataset from a vertical format to a horizontal format. It can be used as a column name when converting a dataset from a vertical to a horizontal format. The value in MKTESTCD cannot be longer than 8 characters, nor can it start with a number (e.g., ""1TEST"" is not valid). MKTESTCD cannot contain characters other than letters, numbers, or underscores. Examples: ""TNDRIND"", ""SWLLIND"", ""SGJSNSCR"".",10,Findings,Req,(MUSCTSCD),MK,
Synonym Qualifier,MK,MKTEST,Name of Musculoskeletal Test,Char,TEST,"Long name For MKTESTCD. Examples: ""Tenderness Indicator"", ""Swollen Indicator"", ""Sharp/Genant JSN Score"".",11,Findings,Req,(MUSCTS),MK,
Grouping Qualifier,MK,MKCAT,Category for Musculoskeletal Test,Char,CAT,Used to define a category of topic-variable values. Examples: "SWOLLEN/TENDER JOINT ASSESSMENT".,12,Findings,Perm,,MK,
Grouping Qualifier,MK,MKSCAT,Subcategory for Musculoskeletal Test,Char,SCAT,Used to define a further categorization of MKCAT values.,13,Findings,Perm,,MK,
Record Qualifier,MK,MKPOS,Position of Subject,Char,POS,"Position of the subject during a measurement or examination. Examples: ""SUPINE"", ""STANDING"", ""SITTING"".",14,Findings,Perm,(POSITION),MK,
Result Qualifier,MK,MKORRES,Result or Finding in Original Units,Char,ORRES,Result of the measurement or finding as originally received or collected.,15,Findings,Exp,,MK,
Variable Qualifier,MK,MKORRESU,Original Units,Char,ORRESU,Unit for MKORRES.,16,Findings,Perm,(UNIT),MK,
Result Qualifier,MK,MKSTRESC,Character Result/Finding in Std Format,Char,STRESC,"Contains the result value for all findings, copied or derived from MKORRES in a standard format or in standard units. MKSTRESC should store all results or findings in character format; if results are numeric, they should also be stored in numeric format in MKSTRESN. For example, if various tests have results ""NONE"", ""NEG"", and ""NEGATIVE"" in MKORRES and these results effectively have the same meaning, they could be represented in standard format in MKSTRESC as ""NEGATIVE"".",17,Findings,Exp,,MK,
Result Qualifier,MK,MKSTRESN,Numeric Result/Finding in Standard Units,Num,STRESN,Used for continuous or numeric results or findings in standard format; copied in numeric format from MKSTRESC. MKSTRESN should store all numeric test results or findings.,18,Findings,Perm,,MK,
Variable Qualifier,MK,MKSTRESU,Standard Units,Char,STRESU,Standardized units used for MKSTRESC and MKSTRESN.,19,Findings,Perm,(UNIT),MK,
Record Qualifier,MK,MKSTAT,Completion Status,Char,STAT,"Used to indicate that a question was not asked or a test was not done, or that a test was attempted but did not generate a result. Should be null if a result exists in MKORRES.",20,Findings,Perm,(ND),MK,
Record Qualifier,MK,MKREASND,Reason Not Done,Char,REASND,Reason not done. Used in conjunction with MKSTAT when value is "NOT DONE".,21,Findings,Perm,,MK,
Record Qualifier,MK,MKLOC,Location Used for the Measurement,Char,LOC,"Anatomical location of the subject relevant to the collection of the measurement. Examples: ""INTERPHALANGEAL JOINT 1"", ""SHOULDER JOINT"".",22,Findings,Exp,(LOC),MK,
Variable Qualifier,MK,MKLAT,Laterality,Char,LAT,"Qualifier for anatomical location or specimen further detailing laterality. Examples: ""RIGHT"", ""LEFT"", ""BILATERAL"".",23,Findings,Perm,(LAT),MK,
Variable Qualifier,MK,MKDIR,Directionality,Char,DIR,"Qualifier for anatomical location further detailing directionality. Examples: ""ANTERIOR"", ""LOWER"", ""PROXIMAL"".",24,Findings,Perm,(DIR),MK,
Record Qualifier,MK,MKMETHOD,Method of Test or Examination,Char,METHOD,"Method of the test or examination. Examples: ""X-RAY"", ""MRI"", ""CT SCAN"".",25,Findings,Perm,(METHOD),MK,
Record Qualifier,MK,MKLOBXFL,Last Observation Before Exposure Flag,Char,LOBXFL,Operationally-derived indicator used to identify the last non-missing value prior to RFXSTDTC. The value should be "Y" or null.,26,Findings,Exp,(NY),MK,
Record Qualifier,MK,MKBLFL,Baseline Flag,Char,BLFL,Indicator used to identify a baseline value. Should be "Y" or null. Note that MKBLFL is retained for backward compatibility. The authoritative baseline for statistical analysis is in an ADaM dataset.,27,Findings,Perm,(NY),MK,
Record Qualifier,MK,MKDRVFL,Derived Flag,Char,DRVFL,"Used to indicate a derived record (e.g., a record that represents the average of other records such as a computed baseline). Should be ""Y"" or null.",28,Findings,Perm,(NY),MK,
Record Qualifier,MK,MKEVAL,Evaluator,Char,EVAL,"Role of the person who provided the evaluation. Used only for results that are subjective (e.g., assigned by a person or a group). Examples: ""ADJUDICATION COMMITTEE"", ""INDEPENDENT ASSESSOR"", ""RADIOLOGIST"".",29,Findings,Perm,(EVAL),MK,
Variable Qualifier,MK,MKEVALID,Evaluator Identifier,Char,EVALID,Used to distinguish multiple evaluators with the same role recorded in MKEVAL. Examples: "RADIOLOGIST1" or "RADIOLOGIST2".,30,Findings,Perm,(MEDEVAL),MK,
Timing,MK,VISITNUM,Visit Number,Num,VISITNUM,"Clinical encounter number. Numeric version of VISIT, used for sorting.",31,Findings,Exp,,,
Timing,MK,VISIT,Visit Name,Char,VISIT,Protocol-defined description of a clinical encounter.,32,Findings,Perm,,,
Timing,MK,VISITDY,Planned Study Day of Visit,Num,VISITDY,Planned study day of VISIT. Should be an integer.,33,Findings,Perm,,,
Timing,MK,TAETORD,Planned Order of Element within Arm,Num,TAETORD,Number that gives the planned order of the Element within the Arm for the Element in which the assessment was made.,34,Findings,Perm,,,
Timing,MK,EPOCH,Epoch,Char,EPOCH,Epoch associated with the date/time at which the assessment was made.,35,Findings,Perm,(EPOCH),,
Timing,MK,MKDTC,Date/Time of Collection,Char,DTC,Collection date and time of an observation.,36,Findings,Exp,ISO 8601,MK,
Timing,MK,MKDY,Study Day of Visit/Collection/Exam,Num,DY,Actual study day of visit/collection/exam expressed in integer days relative to the sponsor-defined RFSTDTC in Demographics.,37,Findings,Perm,,MK,
Timing,MK,MKTPT,Planned Time Point Name,Char,TPT,"Text description of time when a measurement or observation should be taken as defined in the protocol. This may be represented as an elapsed time relative to a fixed reference point, such as time of last dose. See MKTPTNUM and MKTPTREF.",38,Findings,Perm,,MK,
Timing,MK,MKTPTNUM,Planned Time Point Number,Num,TPTNUM,Numeric version of planned time point used in sorting.,39,Findings,Perm,,MK,
Timing,MK,MKELTM,Planned Elapsed Time from Time Point Ref,Char,ELTM,"Planned Elapsed time relative to a planned fixed reference (MKTPTREF) such as ""Previous Dose"" or ""Previous Meal"". This variable is useful where there are repetitive measures. Not a clock time or a date/time variable, but an interval, represented as ISO duration.",40,Findings,Perm,ISO 8601,MK,
Timing,MK,MKTPTREF,Time Point Reference,Char,TPTREF,"Description of the fixed reference point referred to by MKELTM, MKTPTNUM, and MKTPT. Examples: ""PREVIOUS DOSE"", ""PREVIOUS MEAL"".",41,Findings,Perm,,MK,
Timing,MK,MKRFTDTC,Date/Time of Reference Time Point,Char,RFTDTC,Date/time for a fixed reference time point defined by MKTPTREF.,42,Findings,Perm,ISO 8601,MK,
Identifier,,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,43,Findings,Req,,,
Identifier,,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,44,Findings,Req,,,
Identifier,,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product.,45,Findings,Req,,,
Identifier,,--SEQ,Sequence Number,Num,SEQ,"Sequence number to ensure uniqueness of records within a dataset for a subject (or within a parameter, in the case of the Trial Summary domain). May be any valid number (including decimals) and does not have to start at 1.",46,Findings,Req,,,
Topic,,--TESTCD,"Short Name of Measurement, Test or Exam",Char,TESTCD,Short character value for --TEST used as a column name when converting a dataset from a vertical format to a horizontal format. The short value can be up to 8 characters. \n Subject to Domain-specific test code controlled terminology.,47,Findings,Req,,,
Synonym Qualifier,,--TEST,"Name of Measurement, Test or Examination",Char,TEST,Long name for --TESTCD. \n Subject to Domain-specific test code controlled terminology.,48,Findings,Req,,,
Result Qualifier,,--ORRES,Result or Finding in Original Units,Char,ORRES,Result of the measurement or finding as originally received or collected.,49,Findings,Exp,,,
Result Qualifier,,--STRESC,Result or Finding in Standard Format,Char,STRESC,"Contains the result value for all findings, copied or derived from --ORRES in a standard format or in standard units. --STRESC should store all results or findings in character format; if results are numeric, they should also be stored in numeric format in --STRESN. For example, if various tests have results &quot;NONE&quot;, &quot;NEG&quot;, and &quot;NEGATIVE&quot; in --ORRES, and these results effectively have the same meaning, they could be represented in standard format in --STRESC as &quot;NEGATIVE&quot;.",50,Findings,Exp,,,
Record Qualifier,,--LOBXFL,Last Observation Before Exposure Flag,Char,LOBXFL,Operationally-derived indicator used to identify the last non-missing value prior to RFXSTDTC. The value should be &quot;Y&quot; or null.,51,Findings,Exp,,,
Timing,,VISITNUM,Visit Number,Num,VISITNUM,"1. Clinical encounter number. \n 2. Numeric version of VISIT, used for sorting.",52,Findings,Exp,,,
Timing,,--DTC,Date/Time of Collection,Char,DTC,Collection date and time of an observation.,53,Findings,Exp,ISO 8601,,
Timing,,--DY,Study Day of Collection,Num,DY,"Study day of the collection, in integer days. The algorithm for calculations must be relative to the sponsor-defined RFSTDTC variable in the Demographics (DM) domain.",54,Findings,Exp,,,
Identifier,MO,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Findings,Req,,,
Identifier,MO,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Findings,Req,MO,,
Identifier,MO,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product.,3,Findings,Req,,,
Identifier,MO,MOSEQ,Sequence Number,Num,SEQ,Sequence number given to ensure uniqueness of subject records within a domain. May be any valid number.,4,Findings,Req,,MO,
Identifier,MO,MOGRPID,Group ID,Char,GRPID,Used to tie together a block of related records in a single domain for a subject.,5,Findings,Perm,,MO,
Identifier,MO,MOREFID,Reference ID,Char,REFID,Internal or external procedure identifier.,6,Findings,Perm,,MO,
Identifier,MO,MOSPID,Sponsor-Defined Identifier,Char,SPID,Sponsor-defined reference number. Perhaps preprinted on the CRF as an explicit line identifier or defined in the sponsor's operational database. Example: Line number from the procedure or test page.,7,Findings,Perm,,MO,
Identifier,MO,MOLNKID,Link ID,Char,LNKID,Identifier used to link results of a procedure to the procedure performed.,8,Findings,Perm,,MO,
Topic,MO,MOTESTCD,Test or Examination Short Name,Char,TESTCD,"Short name of the measurement, test, or examination described in MOTEST. It can be used as a column name when converting a dataset from a vertical to a horizontal format. The value in MOTESTCD cannot be longer than 8 characters, nor can it start with a number (e.g., &quot;1TEST&quot; is not valid). MOTESTCD cannot contain characters other than letters, numbers, or underscores. Examples: &quot;VOLUME&quot;, &quot;INTP&quot;.",9,Findings,Req,,MO,
Synonym Qualifier,MO,MOTEST,Test or Examination Name,Char,TEST,"Verbatim name of the test or examination used to obtain the measurement or finding. The value in MOTEST cannot be longer than 40 characters. Examples: &quot;Volume&quot;, &quot;Interpretation&quot;.",10,Findings,Req,,MO,
Grouping Qualifier,MO,MOCAT,Category for Test,Char,CAT,Used to categorize observations across subjects.,11,Findings,Perm,,MO,
Grouping Qualifier,MO,MOSCAT,Subcategory for Test,Char,SCAT,A further categorization.,12,Findings,Perm,,MO,
Record Qualifier,MO,MOPOS,Position of Subject,Char,POS,"Position of the subject during a measurement or examination. Examples: &quot;SUPINE&quot;, &quot;STANDING&quot;, &quot;SITTING&quot;.",13,Findings,Perm,(POSITION),MO,
Result Qualifier,MO,MOORRES,Result or Finding in Original Units,Char,ORRES,Result of the procedure measurement or finding as originally received or collected.,14,Findings,Exp,,MO,
Variable Qualifier,MO,MOORRESU,Original Units,Char,ORRESU,Original units in which the data were collected. The unit for MOORRES.,15,Findings,Perm,(UNIT),MO,
Result Qualifier,MO,MOSTRESC,Character Result/Finding in Std Format,Char,STRESC,"Contains the result value for all findings, copied or derived from MOORRES in a standard format or standard units. MOSTRESC should store all results or findings in character format; if results are numeric, they should also be stored in numeric format in MOSTRESN.",16,Findings,Exp,,MO,
Result Qualifier,MO,MOSTRESN,Numeric Result/Finding in Standard Units,Num,STRESN,Used for continuous or numeric results or findings in standard format; copied in numeric format from MOSTRESC. MOSTRESN should store all numeric test results or findings.,17,Findings,Perm,,MO,
Variable Qualifier,MO,MOSTRESU,Standard Units,Char,STRESU,Standardized unit used for MOSTRESC or MOSTRESN.,18,Findings,Perm,(UNIT),MO,
Record Qualifier,MO,MOSTAT,Completion Status,Char,STAT,"Used to indicate a test was not done, or a measurement was not taken. Should be null if a result exists in MOORRES.",19,Findings,Perm,(ND),MO,
Record Qualifier,MO,MOREASND,Reason Test Not Performed,Char,REASND,Describes why a measurement or test was not performed. Examples: &quot;BROKEN EQUIPMENT&quot; or &quot;SUBJECT REFUSED&quot;. Used in conjunction with MOSTAT when value is &quot;NOT DONE&quot;.,20,Findings,Perm,,MO,
Record Qualifier,MO,MOXFN,External File Path,Char,XFN,File path to the external file.,21,Findings,Perm,,MO,
Record Qualifier,MO,MONAM,Vendor Name,Char,NAM,Name or identifier of the laboratory or vendor who provided the test results.,22,Findings,Perm,,MO,
Record Qualifier,MO,MOLOC,Location Used for Measurement,Char,LOC,"Location relevant to the collection of the measurement. Examples: &quot;BRAIN&quot;, &quot;KIDNEY&quot;, &quot;LIVER&quot;, etc.",23,Findings,Perm,(LOC),MO,
Variable Qualifier,MO,MOLAT,Specimen Laterality within Subject,Char,LAT,"Qualifier for laterality of the specimen within the subject for paired specimens. Examples: &quot;LEFT&quot;, &quot;RIGHT&quot;, &quot;BILATERAL&quot;.",24,Findings,Perm,(LAT),MO,
Variable Qualifier,MO,MODIR,Specimen Directionality within Subject,Char,DIR,"Qualifier for directionality of the specimen within the subject. Examples: &quot;DORSAL&quot;, &quot;PROXIMAL&quot;.",25,Findings,Perm,(DIR),MO,
Variable Qualifier,MO,MOPORTOT,Portion or Totality,Char,PORTOT,"Qualifier for anatomical location or specimen further detailing the portion of totality which means arrangement of, or apportioning of. Examples: &quot;ENTIRE&quot;, &quot;PARTIAL&quot;.",26,Findings,Perm,(PORTOT),MO,
Record Qualifier,MO,MOMETHOD,Method of Procedure Test,Char,METHOD,Method of the test or examination result.,27,Findings,Perm,(METHOD),MO,
Record Qualifier,MO,MOANMETH,Analysis Method,Char,ANMETH,Analysis method applied to obtain a summarized result. Example: &quot;STEREOLOGY&quot;.,28,Findings,Perm,,MO,
Record Qualifier,MO,MOLOBXFL,Last Observation Before Exposure Flag,Char,LOBXFL,Operationally-derived indicator used to identify the last non-missing value prior to RFXSTDTC. The value should be &quot;Y&quot; or null.,29,Findings,Perm,(NY),MO,
Record Qualifier,MO,MOBLFL,Baseline Flag,Char,BLFL,Indicator used to identify a baseline value. The value should be &quot;Y&quot; or &quot;null&quot;. Note that MOBLFL is retained for backward compatibility. The authoritative baseline flag for statistical analysis is in an ADaM dataset.,30,Findings,Exp,(NY),MO,
Record Qualifier,MO,MODRVFL,Derived Flag,Char,DRVFL,"Used to indicate a derived record. The value should be &quot;Y&quot; or null. Records that represent the average of other records, or that do not come from the CRF, or are not as originally collected or received are examples of records that would be derived for the submission datasets. If MODRVFL = &quot;Y&quot;, then MOORRES could be null, and (if numeric) MOSTRESN have the derived value.",31,Findings,Perm,(NY),MO,
Record Qualifier,MO,MOEVAL,Evaluator,Char,EVAL,"Role of the person who provided the evaluation. Used only for results that are subjective (e.g., assigned by a person or a group). Should be null for records that contain collected or derived data. Examples: &quot;INVESTIGATOR&quot;, &quot;ADJUDICATION COMMITTEE&quot;, &quot;VENDOR&quot;.",32,Findings,Perm,(EVAL),MO,
Timing,MO,VISITNUM,Visit Number,Num,VISITNUM,"1. Clinical encounter number. \n 2. Numeric version of VISIT, used for sorting.",33,Findings,Exp,,,
Timing,MO,VISIT,Visit Name,Char,VISIT,Protocol-defined description of clinical encounter.May be used in addition to VISITNUM and/or VISITDY.,34,Findings,Perm,,,
Timing,MO,VISITDY,Planned Study Day of Visit,Num,VISITDY,Planned study day of the visit based upon RFSTDTC in Demographics.,35,Findings,Perm,,,
Timing,MO,TAETORD,Planned Order of Element within Arm,Num,TAETORD,Number that gives the planned order of the Element within the Arm for the Element in which the assessment was made.,36,Findings,Perm,,,
Timing,MO,EPOCH,Epoch,Char,EPOCH,Epoch associated with the date/time at which the observation was made.,37,Findings,Perm,(EPOCH),,
Timing,MO,MODTC,Date/Time of Test,Char,DTC,Date of test.,38,Findings,Exp,ISO 8601,MO,
Timing,MO,MODY,Study Day of Test,Num,DY,"Study day of the procedure or test, measured as integer days.Algorithm for calculations must be relative to the sponsor-defined RFSTDTC variable in Demographics.",39,Findings,Perm,,MO,
Timing,MO,MOTPT,Planned Time Point Name,Char,TPT,"Text Description of time when measurement should be taken.This may be represented as an elapsed time relative to a fixed reference point, such as time of last dose. See MOTPTNUM and MOTPTREF. Examples: &quot;Start&quot;, &quot;5 min post&quot;.",40,Findings,Perm,,MO,
Timing,MO,MOTPTNUM,Planned Time Point Number,Num,TPTNUM,Numerical version of MOTPT to aid in sorting.,41,Findings,Perm,,MO,
Timing,MO,MOELTM,Planned Elapsed Time from Time Point Ref,Char,ELTM,"Planned elapsed time (in ISO 8601) relative to a fixed time point reference (MOTPTREF). Not a clock time or a date time variable. Represented as an ISO 8601 duration. Examples: &quot;-PT15M&quot; to represent the period of 15 minutes prior to the reference point indicated by MOTPTREF, or &quot;PT8H&quot; to represent the period of 8 hours after the reference point indicated by MOTPTREF.",42,Findings,Perm,ISO 8601,MO,
Timing,MO,MOTPTREF,Time Point Reference,Char,TPTREF,"Name of the fixed reference point referred to by MOELTM, MOTPTNUM, and MOTPT. Examples: &quot;PREVIOUS DOSE&quot;, &quot;PREVIOUS MEAL&quot;.",43,Findings,Perm,,MO,
Timing,MO,MORFTDTC,Date/Time of Reference Time Point,Char,RFTDTC,"Date/time of the reference time point, MOTPTREF.",44,Findings,Perm,ISO 8601,MO,
Identifier,MS,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Findings,Req,,,
Identifier,MS,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Findings,Req,MS,,
Identifier,MS,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product.,3,Findings,Req,,,
Identifier,MS,NHOID,Non-host Organism ID,Char,NHOID,Sponsor-defined identifier for a non-host organism which should only be used when the organism is the subject of the TEST. This variable should be populated with an intuitive name based on the identity of the non-host organism as reported by a lab (Example: "A/California/7/2009 (H1N1)"). It is not to be used as a qualifier of the result in the record on which it appears.,4,Findings,Perm,,,
Identifier,MS,MSSEQ,Sequence Number,Num,SEQ,"Sequence number to ensure uniqueness of records within a dataset for a subject (or within a parameter, in the case of the Trial Summary domain). May be any valid number (including decimals) and does not have to start at 1.",5,Findings,Req,,MS,
Identifier,MS,MSGRPID,Group ID,Char,GRPID,"Optional group identifier, used to link together a block of related records within a subject in a domain. In SDTMIG v3.2 this was an Expected variable. In this version, the core designation has been changed to Permissible.",6,Findings,Perm,,MS,
Identifier,MS,MSREFID,Reference ID,Char,REFID,Optional internal or external identifier such as an identifier for the culture/isolate being tested for susceptibility.,7,Findings,Perm,,MS,
Identifier,MS,MSSPID,Sponsor-Defined Identifier,Char,SPID,Sponsor-defined reference number. Perhaps preprinted on the CRF as an explicit line identifier or defined in the sponsor's operational database.,8,Findings,Perm,,MS,
Identifier,MS,MSLNKID,Link ID,Char,LNKID,"Identifier used to link related records across domains. This may be a one-to-one or a one-to-many relationship. For example, it may be used to link genetic findings (in the PF domain) about a microbe to the original culture of that microbe (in MB), or to susceptibility records (in MS) if needed.",9,Findings,Perm,,MS,
Topic,MS,MSTESTCD,Short Name of Assessment,Char,TESTCD,"Short character value for MSTEST used as a column name when converting a dataset from a vertical format to a horizontal format. It can be used as a column name when converting a dataset from a vertical to a horizontal format. The value in MSTESTCD cannot be longer than 8 characters, nor can it start with a number (e.g., ""1TEST"" is not valid). MSTESTCD cannot contain characters other than letters, numbers, or underscores. Examples: ""MIC"" for Minimum Inhibitory Concentration; ""MICROSUS"" for Microbial Susceptibility.",10,Findings,Req,(MSTESTCD),MS,
Synonym Qualifier,MS,MSTEST,Name of Assessment,Char,TEST,"Verbatim name of the test or examination used to obtain the measurement or finding. The value in MSTEST cannot be longer than 40 characters. Examples: ""Minimum Inhibitory Concentration"", ""Microbial Susceptibility"".",11,Findings,Req,(MSTEST),MS,
Variable Qualifier,MS,MSTSTDTL,"Measurement, Test or Examination Detail",Char,TSTDTL,Further description of MSTESTCD and MSTEST.,12,Findings,Perm,,MS,
Variable Qualifier,MS,MSAGENT,Agent Name,Char,AGENT,"The name of the agent for which resistance is tested. The agent specified may be based on genetic markers or direct phenotypic drug sensitivity testing. Examples: ""Penicillin"", name of study drug.",13,Findings,Exp,,MS,
Synonym Qualifier,MS,MSMODIFY,Modified Reported Name,Char,MODIFY,"If MSAGENT is modified to facilitate coding, then MSMODIFY will contain the modified text.",14,Findings,Perm,,MS,
Variable Qualifier,MS,MSCONC,Agent Concentration,Num,CONC,Numeric concentration of agent listed in MSAGENT.,15,Findings,Perm,,MS,
Variable Qualifier,MS,MSCONCU,Agent Concentration Units,Char,CONCU,Units for value of the agent concentration listed in MSCONC. Example: "mg/L".,16,Findings,Perm,(UNIT),MS,
Grouping Qualifier,MS,MSCAT,Category,Char,CAT,Used to define a category of MSTEST values.,17,Findings,Perm,,MS,
Grouping Qualifier,MS,MSSCAT,Subcategory,Char,SCAT,Used to define a further categorization of MSCAT values.,18,Findings,Perm,,MS,
Result Qualifier,MS,MSORRES,Result or Finding in Original Units,Char,ORRES,Result of the measurement or finding as originally received or collected.,19,Findings,Exp,,MS,
Variable Qualifier,MS,MSORRESU,Original Units,Char,ORRESU,Unit for MSORRES. Examples: "ug/mL".,20,Findings,Perm,(UNIT),MS,
Result Qualifier,MS,MSSTRESC,Result or Finding in Standard Format,Char,STRESC,"Contains the result value for all findings, copied or derived from MSORRES in a standard format or in standard units. MSSTRESC should store all results or findings in character format; if results are numeric, they should also be stored in numeric format in MSSTRESN. For example, if various tests have results ""NONE"", ""NEG"", and ""NEGATIVE"" in MSORRES and these results effectively have the same meaning, they could be represented in standard format in MSSTRESC as ""NEGATIVE"".",21,Findings,Exp,,MS,
Result Qualifier,MS,MSSTRESN,Numeric Result/Finding in Standard Units,Num,STRESN,Used for continuous or numeric results or findings in standard format; copied in numeric format from MSSTRESC. MSSTRESN should store all numeric test results or findings.,22,Findings,Perm,,MS,
Variable Qualifier,MS,MSSTRESU,Standard Units,Char,STRESU,Standardized units used for MSSTRESC and MSSTRESN. Example: "mol/L".,23,Findings,Perm,(UNIT),MS,
Variable Qualifier,MS,MSNRIND,Normal/Reference Range Indicator,Char,NRIND,"Used to indicate the value is outside the normal range or reference range. May be defined by MSORNRLO and MSORNRHI or other objective criteria. Examples: ""Y"", ""N"", ""HIGH"", ""LOW"", ""NORMAL"". ""ABNORMAL"".",24,Findings,Perm,,MS,
Variable Qualifier,MS,MSRESCAT,Result Category,Char,RESCAT,"Used to categorize the result of a finding. In SDTMIG v3.2, MSRESCAT was used to categorize a numeric susceptibility result represented in MSORRES as either ""SUSCEPTIBLE"", ""INTERMEDIATE"", or ""RESISTANT"". However, results from some susceptibility tests may report only a categorical result and not a numeric result. Thus, in order for susceptibility results to be represented consistently, MSRESCAT should no longer be used for this purpose. In this version, the core designation has been changed from Expected to Permissible.",25,Findings,Perm,(MSRESCAT),MS,
Record Qualifier,MS,MSSTAT,Completion Status,Char,STAT,"Used to indicate that a question was not asked or a test was not done, or a test was attempted but did not generate a result. Should be null or have a value of ""NOT DONE"".",26,Findings,Perm,(ND),MS,
Record Qualifier,MS,MSREASND,Reason Not Done,Char,REASND,Reason not done. Used in conjunction with MSSTAT when value is "NOT DONE".,27,Findings,Perm,,MS,
Record Qualifier,MS,MSXFN,External File Path,Char,XFN,Filename for an external file.,28,Findings,Perm,,MS,
Record Qualifier,MS,MSNAM,Laboratory/Vendor Name,Char,NAM,"Name or identifier of the vendor (e.g., laboratory) that provided the test results.",29,Findings,Perm,,MS,
Synonym Qualifier,MS,MSLOINC,LOINC Code,Char,LOINC,Logical Observation Identifiers Names and Codes (LOINC) code for the topic variable such as a lab test.,30,Findings,Perm,,MS,
Record Qualifier,MS,MSSPEC,Specimen Material Type,Char,SPEC,Defines the type of specimen used for a measurement. Examples: "SPUTUM".,31,Findings,Perm,(SPECTYPE),MS,
Record Qualifier,MS,MSSPCCND,Specimen Condition,Char,SPCCND,Defines the condition of the specimen. Example: "CLOUDY".,32,Findings,Perm,(SPECCOND),MS,
Record Qualifier,MS,MSSPCUFL,Specimen Usability for the Test,Char,SPCUFL,"Describes the usability of the specimen for the test. The value will be ""N"" if the specimen is not usable, and null if the specimen is usable.",33,Findings,Perm,(NY),MS,
Record Qualifier,MS,MSLOC,Location Used for the Measurement,Char,LOC,Anatomical location of the subject relevant to the collection of the measurement.,34,Findings,Perm,(LOC),MS,
Variable Qualifier,MS,MSLAT,Laterality,Char,LAT,"Qualifier for anatomical location or specimen further detailing laterality. Examples: ""RIGHT"", ""LEFT"", ""BILATERAL"".",35,Findings,Perm,(LAT),MS,
Variable Qualifier,MS,MSDIR,Directionality,Char,DIR,"Qualifier for anatomical location or specimen further detailing directionality. Examples: ""ANTERIOR"", ""LOWER"", ""PROXIMAL"".",36,Findings,Perm,(DIR),MS,
Record Qualifier,MS,MSMETHOD,Method of Test or Examination,Char,METHOD,"Method of the test or examination. Examples: ""EPSILOMETER"", ""MACRO BROTH DILUTION"".",37,Findings,Perm,(METHOD),MS,
Record Qualifier,MS,MSANMETH,Analysis Method,Char,ANMETH,Analysis method applied to obtain a summarized result. Analysis method describes the method of secondary processing applied to a complex observation result (e.g. an image or a genetic sequence).,38,Findings,Perm,,MS,
Record Qualifier,MS,MSLOBXFL,Last Observation Before Exposure Flag,Char,LOBXFL,Operationally-derived indicator used to identify the last non-missing value prior to RFXSTDTC. The value should be "Y" or null.,39,Findings,Perm,(NY),MS,
Record Qualifier,MS,MSBLFL,Baseline Flag,Char,BLFL,Indicator used to identify a baseline value. Should be "Y" or null. Note that MSBLFL is retained for backward compatibility. The authoritative baseline for statistical analysis is in an ADaM dataset.,40,Findings,Perm,(NY),MS,
Record Qualifier,MS,MSFAST,Fasting Status,Char,FAST,"Indicator used to identify fasting status. Valid values include ""Y"", ""N"", ""U"" or null if not relevant.",41,Findings,Perm,(NY),MS,
Record Qualifier,MS,MSDRVFL,Derived Flag,Char,DRVFL,"Used to indicate a derived record (e.g., a record that represents the average of other records such as a computed baseline). Should be ""Y"" or null.",42,Findings,Perm,(NY),MS,
Record Qualifier,MS,MSEVAL,Evaluator,Char,EVAL,"Role of the person who provided the evaluation. Used only for results that are subjective (e.g., assigned by a person or a group). Examples: ""ADJUDICATION COMMITTEE"", ""INDEPENDENT ASSESSOR"", ""MICROSCOPIST"".",43,Findings,Perm,(EVAL),MS,
Variable Qualifier,MS,MSEVALID,Evaluator Identifier,Char,EVALID,Used to distinguish multiple evaluators with the same role recorded in MSEVAL. Examples: "RADIOLOGIST1" or "RADIOLOGIST2".,44,Findings,Perm,(MEDEVAL),MS,
Record Qualifier,MS,MSACPTFL,Accepted Record Flag,Char,ACPTFL,"In cases where more than one assessor provides an evaluation of a result or response, this flag identifies the record that is considered, by an independent assessor, to be the accepted evaluation. Expected to be ""Y"" or null.",45,Findings,Perm,(NY),MS,
Variable Qualifier,MS,MSLLOQ,Lower Limit of Quantitation,Num,LLOQ,Indicates the lower limit of quantitation for an assay. Units will be those used for MSSTRESU.,46,Findings,Perm,,MS,
Variable Qualifier,MS,MSULOQ,Upper Limit of Quantitation,Num,ULOQ,Indicates the upper limit of quantitation for an assay. Units will be those used for MSSTRESU.,47,Findings,Perm,,MS,
Record Qualifier,MS,MSREPNUM,Repetition Number,Num,REPNUM,"The incidence number of a test that is repeated within a given timeframe for the same test. The level of granularity can vary, e.g., within a time point or within a visit. For example, multiple measurements of blood pressure or multiple analyses of a sample.",48,Findings,Perm,,MS,
Timing,MS,VISITNUM,Visit Number,Num,VISITNUM,"Clinical encounter number. Numeric version of VISIT, used for sorting.",49,Findings,Exp,,,
Timing,MS,VISIT,Visit Name,Char,VISIT,Protocol-defined description of a clinical encounter.,50,Findings,Perm,,,
Timing,MS,VISITDY,Planned Study Day of Visit,Num,VISITDY,Planned study day of VISIT. Should be an integer.,51,Findings,Perm,,,
Timing,MS,TAETORD,Planned Order of Element within Arm,Num,TAETORD,Number that gives the planned order of the Element within the Arm for the element in which the specimen was collected.,52,Findings,Perm,,,
Timing,MS,EPOCH,Epoch,Char,EPOCH,Epoch associated with the date/time at which the specimen was collected.,53,Findings,Perm,(EPOCH),,
Timing,MS,MSDTC,Date/Time of Collection,Char,DTC,Collection date and time of an observation.,54,Findings,Perm,ISO 8601,MS,
Timing,MS,MSENDTC,End Date/Time of Observation,Char,ENDTC,End date/time of the observation.,55,Findings,Perm,ISO 8601,MS,
Timing,MS,MSDY,Study Day of Visit/Collection/Exam,Num,DY,Actual study day of visit/collection/exam expressed in integer days relative to the sponsor-defined RFSTDTC in Demographics.,56,Findings,Perm,,MS,
Timing,MS,MSENDY,Study Day of End of Observation,Num,ENDY,Actual study day of end of observation expressed in integer days relative to the sponsor-defined RFSTDTC in Demographics.,57,Findings,Perm,,MS,
Timing,MS,MSDUR,Duration,Char,DUR,"Collected duration of an event, intervention, or finding. Used only if collected on the CRF and not derived.",58,Findings,Perm,ISO 8601,MS,
Timing,MS,MSTPT,Planned Time Point Name,Char,TPT,"Text description of time when a measurement or observation should be taken as defined in the protocol. This may be represented as an elapsed time relative to a fixed reference point, such as time of last dose. See MSTPTNUM and MSTPTREF.",59,Findings,Perm,,MS,
Timing,MS,MSTPTNUM,Planned Time Point Number,Num,TPTNUM,Numeric version of planned time point used in sorting.,60,Findings,Perm,,MS,
Timing,MS,MSELTM,Planned Elapsed Time from Time Point Ref,Char,ELTM,"Planned Elapsed time relative to a planned fixed reference (MSTPTREF) such as ""Previous Dose"" or ""Previous Meal"". This variable is useful where there are repetitive measures. Not a clock time or a date/time variable, but an interval, represented as ISO duration.",61,Findings,Perm,ISO 8601,MS,
Timing,MS,MSTPTREF,Time Point Reference,Char,TPTREF,"Description of the fixed reference point referred to by MSELTM, MSTPTNUM, and MSTPT. Example: ""PREVIOUS DOSE"".",62,Findings,Perm,,MS,
Timing,MS,MSRFTDTC,Date/Time of Reference Time Point,Char,RFTDTC,Date/time for a fixed reference time point defined by MSTPTREF.,63,Findings,Perm,ISO 8601,MS,
Timing,MS,MSSTRF,Start Relative to Reference Period,Char,STRF,"Identifies the start of the observation as being before, during, or after the sponsor-defined reference period. The sponsor-defined reference period is a continuous period of time defined by a discrete starting point and a discrete ending point represented by RFSTDTC and RFENDTC in Demographics.",64,Findings,Perm,(STENRF),MS,
Timing,MS,MSENRF,End Relative to Reference Period,Char,ENRF,"Identifies the end of the observation as being before, during or after the sponsor-defined reference period. The sponsor-defined reference period is a continuous period of time defined by a discrete starting point and a discrete ending point represented by RFSTDTC and RFENDTC in Demographics.",65,Findings,Perm,(STENRF),MS,
Timing,MS,MSEVLINT,Evaluation Interval,Char,EVLINT,Duration of interval associated with an observation such as a finding MSTESTCD. Example: "-P2M" to represent a period of the past 2 months before the assessment.,66,Findings,Perm,ISO 8601,MS,
Timing,MS,MSEVINTX,Evaluation Interval Text,Char,EVINTX,"Evaluation interval associated with an observation, where the interval is not able to be represented in ISO 8601 format. Examples: ""LIFETIME"", ""LAST NIGHT"", ""RECENTLY"", ""OVER THE LAST FEW WEEKS"".",67,Findings,Perm,,MS,
Timing,MS,MSSTRTPT,Start Relative to Reference Time Point,Char,STRTPT,Identifies the start of the observation as being before or after the sponsor-defined reference time point defined by variable MSSTTPT.,68,Findings,Perm,(STENRF),MS,
Timing,MS,MSSTTPT,Start Reference Time Point,Char,STTPT,"Description or date/time, in ISO 8601 or other character format, of the sponsor-defined reference point referred to by MSSTRTPT. Examples: ""2003-12-15"" or ""VISIT 1"".",69,Findings,Perm,,MS,
Timing,MS,MSENRTPT,End Relative to Reference Time Point,Char,ENRTPT,Identifies the end of the observation as being before or after the sponsor-defined reference time point defined by variable MSENTPT.,70,Findings,Perm,(STENRF),MS,
Timing,MS,MSENTPT,End Reference Time Point,Char,ENTPT,Description or date/time in ISO 8601 or other character format of the sponsor-defined reference point referred to by MSENRTPT. Examples: "2003-12-25" or "VISIT 2".,71,Findings,Perm,,MS,
Identifier,NV,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Findings,Req,,,
Identifier,NV,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Findings,Req,NV,,
Identifier,NV,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product.,3,Findings,Req,,,
Identifier,NV,FOCID,Focus of Study-Specific Interest,Char,FOCID,"Identification of a focus of study-specific interest on or within a subject or specimen as called out in the protocol for which a measurement, test, or examination was performed, such as a drug application site, e.g., &quot;Injection site 1&quot;, &quot;Biopsy site 1&quot;, &quot;Treated site 1&quot;, or a more specific focus, e.g., &quot;OD&quot; (right eye) or &quot;Upper left quadrant of the back&quot;. The value in this variable should have inherent semantic meaning.",4,Findings,Perm,,,
Identifier,NV,NVSEQ,Sequence Number,Num,SEQ,Sequence number given to ensure uniqueness of subject records within a domain. May be any valid number.,5,Findings,Req,,NV,
Identifier,NV,NVGRPID,Group ID,Char,GRPID,Used to tie together a block of related records in a single domain for a subject.,6,Findings,Perm,,NV,
Identifier,NV,NVREFID,Reference ID,Char,REFID,Internal or external procedure identifier.,7,Findings,Perm,,NV,
Identifier,NV,NVSPID,Sponsor-Defined Identifier,Char,SPID,Sponsor-defined reference number. Perhaps preprinted on the CRF as an explicit line identifier or defined in the sponsor's operational database. Example: Line number from the procedure or test page.,8,Findings,Perm,,NV,
Identifier,NV,NVLNKID,Link ID,Char,LNKID,Identifier used to link a procedure to the assessment results over the course of the study.,9,Findings,Perm,,NV,
Identifier,NV,NVLNKGRP,Link Group,Char,LNKGRP,Identifier used to link related records across domains. This will usually be a many-to-one relationship.,10,Findings,Perm,,NV,
Topic,NV,NVTESTCD,Short Name of Nervous System Test,Char,TESTCD,"Short name of the measurement, test, or examination described in NVTEST. It can be used as a column name when converting a dataset from a vertical to a horizontal format. The value in NVTESTCD cannot be longer than 8 characters, nor can it start with a number (e.g., &quot;1TEST&quot; is not valid). NVTESTCD cannot contain characters other than letters, numbers, or underscores. Example: &quot;SUVR&quot;, &quot;N75LAT&quot;, &quot;P100LAT&quot;,&quot;N145LAT&quot;, etc.",11,Findings,Req,(NVTESTCD),NV,
Synonym Qualifier,NV,NVTEST,Name of Nervous System Test,Char,TEST,"Verbatim name of the test or examination used to obtain the measurement or finding. The value in NVTEST cannot be longer than 40 characters. Example: &quot;Standard Uptake Value Ratio&quot;, &quot;N75 Latency&quot;, &quot;P100 Latency&quot;, &quot;N145 Latency&quot;, etc.",12,Findings,Req,(NVTEST),NV,
Grouping Qualifier,NV,NVCAT,Category for Nervous System Test,Char,CAT,Used to define a category of topic-variable values. Example: &quot;VISUAL EVOKED POTENTIAL&quot;.,13,Findings,Perm,,NV,
Grouping Qualifier,NV,NVSCAT,Subcategory for Nervous System Test,Char,SCAT,Used to define a further categorization of NVCAT values.,14,Findings,Perm,,NV,
Result Qualifier,NV,NVORRES,Result or Finding in Original Units,Char,ORRES,Result of the procedure measurement or finding as originally received or collected.,15,Findings,Exp,,NV,
Variable Qualifier,NV,NVORRESU,Original Units,Char,ORRESU,Original units in which the data were collected. The unit for NVORRES.,16,Findings,Perm,(UNIT),NV,
Result Qualifier,NV,NVSTRESC,Character Result/Finding in Std Format,Char,STRESC,"Contains the result value for all findings, copied or derived from NVORRES in a standard format or standard units. NVSTRESC should store all results or findings in character format; if results are numeric, they should also be stored in numeric format in NVSTRESN.",17,Findings,Exp,,NV,
Result Qualifier,NV,NVSTRESN,Numeric Result/Finding in Standard Units,Num,STRESN,Used for continuous or numeric results or findings in standard format; copied in numeric format from NVSTRESC. NVSTRESN should store all numeric test results or findings.,18,Findings,Perm,,NV,
Variable Qualifier,NV,NVSTRESU,Standard Units,Char,STRESU,Standardized unit used for NVSTRESC or NVSTRESN.,19,Findings,Perm,(UNIT),NV,
Record Qualifier,NV,NVSTAT,Completion Status,Char,STAT,"Used to indicate a test was not done, or a measurement was not taken. Should be null if a result exists in NVORRES.",20,Findings,Perm,(ND),NV,
Record Qualifier,NV,NVREASND,Reason Not Done,Char,REASND,Describes why a measurement or test was not performed. Examples: &quot;BROKEN EQUIPMENT&quot; or &quot;SUBJECT REFUSED&quot;. Used in conjunction with NVSTAT when value is &quot;NOT DONE&quot;.,21,Findings,Perm,,NV,
Record Qualifier,NV,NVLOC,Location Used for the Measurement,Char,LOC,"Anatomical location of the subject relevant to the collection of the measurement. Examples: &quot;BRAIN&quot;, &quot;EYE&quot;, &quot;PRECUNEUS&quot;, &quot;CINGULATE CORTEX&quot;, etc.",22,Findings,Perm,(LOC),NV,
Variable Qualifier,NV,NVLAT,Laterality,Char,LAT,"Qualifier for anatomical location or specimen further detailing laterality. Examples: &quot;RIGHT&quot;, &quot;LEFT&quot;, &quot;BILATERAL&quot;.",23,Findings,Perm,(LAT),NV,
Variable Qualifier,NV,NVDIR,Directionality,Char,DIR,"Qualifier for anatomical location or specimen further detailing directionality. Examples: &quot;ANTERIOR&quot;, &quot;LOWER&quot;, &quot;PROXIMAL&quot;.",24,Findings,Perm,(DIR),NV,
Record Qualifier,NV,NVMETHOD,Method of Test or Examination,Char,METHOD,"Method of the test or examination. Examples: &quot;EEG&quot;, &quot;PET/CT SCAN &quot;, &quot;FDGPET&quot;, etc.",25,Findings,Perm,(METHOD),NV,
Record Qualifier,NV,NVLOBXFL,Last Observation Before Exposure Flag,Char,LOBXFL,Operationally-derived indicator used to identify the last non-missing value prior to RFXSTDTC. The value should be &quot;Y&quot; or null.,26,Findings,Perm,(NY),NV,
Record Qualifier,NV,NVBLFL,Baseline Flag,Char,BLFL,Indicator used to identify a baseline value. Should be &quot;Y&quot; or null. Note that NVBLFL is retained for backward compatibility. The authoritative baseline flag for statistical analysis is in an ADaM dataset.,27,Findings,Perm,(NY),NV,
Record Qualifier,NV,NVDRVFL,Derived Flag,Char,DRVFL,"Used to indicate a derived record (e.g., a record that represents the average of other records such as a computed baseline). Should be &quot;Y&quot; or null.",28,Findings,Perm,(NY),NV,
Record Qualifier,NV,NVEVAL,Evaluator,Char,EVAL,"Role of the person who provided the evaluation. Used only for results that are subjective (e.g., assigned by a person or a group). Examples: &quot;ADJUDICATION COMMITTEE&quot;, &quot;INDEPENDENT ASSESSOR&quot;, &quot;RADIOLOGIST&quot;.",29,Findings,Perm,(EVAL),NV,
Variable Qualifier,NV,NVEVALID,Evaluator Identifier,Char,EVALID,Used to distinguish multiple evaluators with the same role recorded in NVEVAL. Examples: &quot;RADIOLOGIST 1&quot; or &quot;RADIOLOGIST 2&quot;.,30,Findings,Perm,(MEDEVAL),NV,
Timing,NV,VISITNUM,Visit Number,Num,VISITNUM,"1. Clinical encounter number. \n 2. Numeric version of VISIT, used for sorting.",31,Findings,Exp,,,
Timing,NV,VISIT,Visit Name,Char,VISIT,Protocol-defined description of clinical encounter.May be used in addition to VISITNUM and/or VISITDY.,32,Findings,Perm,,,
Timing,NV,VISITDY,Planned Study Day of Visit,Num,VISITDY,Planned study day of the visit based upon RFSTDTC in Demographics.,33,Findings,Perm,,,
Timing,NV,TAETORD,Planned Order of Element within Arm,Num,TAETORD,Number that gives the planned order of the Element within the Arm for the Element in which the assessment was made.,34,Findings,Perm,,,
Timing,NV,EPOCH,Epoch,Char,EPOCH,Epoch associated with the date/time at which the assessment was made.,35,Findings,Perm,(EPOCH),,
Timing,NV,NVDTC,Date/Time of Collection,Char,DTC,Date of procedure or test.,36,Findings,Exp,ISO 8601,NV,
Timing,NV,NVDY,Study Day of Visit/Collection/Exam,Num,DY,"Study day of the procedure or test, measured as integer days.Algorithm for calculations must be relative to the sponsor-defined RFSTDTC variable in Demographics.",37,Findings,Perm,,NV,
Timing,NV,NVTPT,Planned Time Point Name,Char,TPT,"Text description of time when measurement should be taken.This may be represented as an elapsed time relative to a fixed reference point, such as time of last dose. See NVTPTNUM and NVTPTREF. Examples: &quot;Start&quot;, &quot;5 min post&quot;.",38,Findings,Perm,,NV,
Timing,NV,NVTPTNUM,Planned Time Point Number,Num,TPTNUM,Numerical version of NVTPT to aid in sorting.,39,Findings,Perm,,NV,
Timing,NV,NVELTM,Planned Elapsed Time from Time Point Ref,Char,ELTM,"Planned elapsed time (in ISO 8601) relative to a fixed time point reference (NVTPTREF). Not a clock time or a date time variable. Represented as an ISO 8601 duration. Examples: &quot;-PT15M&quot; to represent the period of 15 minutes prior to the reference point indicated by NVTPTREF, or &quot;PT8H&quot; to represent the period of 8 hours after the reference point indicated by NVTPTREF.",40,Findings,Perm,ISO 8601,NV,
Timing,NV,NVTPTREF,Time Point Reference,Char,TPTREF,"Name of the fixed reference point referred to by NVELTM, NVTPTNUM, and NVTPT. Examples: &quot;PREVIOUS DOSE&quot;, &quot;PREVIOUS MEAL&quot;.",41,Findings,Perm,,NV,
Timing,NV,NVRFTDTC,Date/Time of Reference Time Point,Char,RFTDTC,Date/time for a fixed reference time point defined by --TPTREF in ISO 8601 character format.,42,Findings,Perm,ISO 8601,NV,
Identifier,OE,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Findings,Req,,,
Identifier,OE,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Findings,Req,OE,,
Identifier,OE,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product.,3,Findings,Req,,,
Identifier,OE,FOCID,Focus of Study-Specific Interest,Char,FOCID,"Identification of a focus of study-specific interest on or within a subject or specimen as called out in the protocol for which a measurement, test, or examination was performed.",4,Findings,Perm,(OEFOCUS),,
Identifier,OE,OESEQ,Sequence Number,Num,SEQ,Sequence number given to ensure uniqueness of subject records within a domain. May be any valid number.,5,Findings,Req,,OE,
Identifier,OE,OEGRPID,Group ID,Char,GRPID,"Optional group identifier, used to link together a block of related records within a subject in a domain.",6,Findings,Perm,,OE,
Identifier,OE,OELNKID,Link ID,Char,LNKID,Identifier used to link related records across domains. This may be a one-to-one or a one-to-many relationship.,7,Findings,Perm,,OE,
Identifier,OE,OELNKGRP,Link Group,Char,LNKGRP,Identifier used to link related records across domains. This will usually be a many-to-one relationship.,8,Findings,Perm,,OE,
Topic,OE,OETESTCD,Short Name of Ophthalmic Test or Exam,Char,TESTCD,"Short character value for OETEST used as a column name when converting a dataset from a vertical format to a horizontal format. It can be used as a column name when converting a dataset from a vertical to a horizontal format. The value in OETESTCD cannot be longer than 8 characters, nor can it start with a number (e.g., ""1TEST"" is not valid). OETESTCD cannot contain characters other than letters, numbers, or underscores. Example: ""NUMLCOR"".",9,Findings,Req,(OETESTCD),OE,
Synonym Qualifier,OE,OETEST,Name of Ophthalmic Test or Exam,Char,TEST,Long name for the test or examination used to obtain the measurement or finding. The value in OETEST cannot be longer than 40 characters. Example: Number of Letters Correct for OETESTCD = "NUMLCOR".,10,Findings,Req,(OETEST),OE,
Variable Qualifier,OE,OETSTDTL,Ophthalmic Test or Exam Detail,Char,TSTDTL,Further description of OETESTCD and OETEST.,11,Findings,Perm,,OE,
Grouping Qualifier,OE,OECAT,Category for Ophthalmic Test or Exam,Char,CAT,"Used to define a category of topic-variable values. Examples: ""VISUAL ACUITY"", ""CONTRAST SENSITIVIY"", ""OCULAR COMFORT"".",12,Findings,Perm,,OE,
Grouping Qualifier,OE,OESCAT,Subcategory for Ophthalmic Test or Exam,Char,SCAT,Used to define a further categorization of OECAT values. Examples: "HIGH CONTRAST" and "LOW CONTRAST" when OECAT is "VISUAL ACUITY".,13,Findings,Perm,,OE,
Result Qualifier,OE,OEORRES,Result or Finding in Original Units,Char,ORRES,"Result of the measurement or finding as originally received or collected. Examples: ""120"", ""<1, NORMAL"", ""RED SPOT VISIBLE"".",14,Findings,Exp,,OE,
Variable Qualifier,OE,OEORRESU,Original Units,Char,ORRESU,"Original unit for OEORRES. Examples: ""mm"", ""um"".",15,Findings,Exp,(UNIT),OE,
Variable Qualifier,OE,OEORNRLO,Normal Range Lower Limit-Original Units,Char,ORNRLO,Lower end of normal range or reference range for results stored in OEORRES.,16,Findings,Perm,,OE,
Variable Qualifier,OE,OEORNRHI,Normal Range Upper Limit-Original Units,Char,ORNRHI,Upper end of normal range or reference range for results stored in OEORRES.,17,Findings,Perm,,OE,
Result Qualifier,OE,OESTRESC,Character Result/Finding in Std Format,Char,STRESC,"Contains the result value for all findings, copied or derived from OEORRES in a standard format or in standard units. OESTRESC should store all results or findings in character format; if results are numeric, they should also be stored in numeric format in OESTRESN.",18,Findings,Exp,,OE,
Result Qualifier,OE,OESTRESN,Numeric Result/Finding in Standard Units,Num,STRESN,Used for continuous or numeric results or findings in standard format; copied in numeric format from OESTRESC. OESTRESN should store all numeric test results or findings.,19,Findings,Exp,,OE,
Variable Qualifier,OE,OESTRESU,Standard Units,Char,STRESU,"Standardized units used for OESTRESC and OESTRESN. Examples: ""mm"", ""um"".",20,Findings,Exp,(UNIT),OE,
Variable Qualifier,OE,OESTNRLO,Normal Range Lower Limit-Standard Units,Num,STNRLO,"Lower end of normal range or reference range for standardized results (e.g., OESTRESC, OESTRESN) represented in standardized units (OESTRESU).",21,Findings,Perm,,OE,
Variable Qualifier,OE,OESTNRHI,Normal Range Upper Limit-Standard Units,Num,STNRHI,"Upper end of normal range or reference range for standardized results (e.g., OESTRESC, OESTRESN) represented in standardized units (OESTRESU).",22,Findings,Perm,,OE,
Variable Qualifier,OE,OESTNRC,Normal Range for Character Results,Char,STNRC,Normal range or reference range for results stored in OESTRESC that are character in ordinal or categorical scale. Example: "Negative to Trace".,23,Findings,Perm,,OE,
Variable Qualifier,OE,OENRIND,Normal/Reference Range Indicator,Char,NRIND,"Used to indicate the value is outside the normal range or reference range. May be defined by OEORNRLO and OEORNRHI or other objective criteria. Examples: ""Y"", ""N""; ""HIGH"", ""LOW"", ""NORMAL"", ""ABNORMAL"".",24,Findings,Perm,(NRIND),OE,
Variable Qualifier,OE,OERESCAT,Result Category,Char,RESCAT,"Used to categorize the result of a finding or medical status per interpretation of test results. Examples: ""POSITIVE"", ""NEGATIVE"". The variable OERESCAT is not meant to replace the use of OENRIND for cases where normal ranges are provided.",25,Findings,Perm,,OE,
Record Qualifier,OE,OESTAT,Completion Status,Char,STAT,"Used to indicate that a question was not asked or a test was not done, or a test was attempted but did not generate a result. Should be null or have a value of ""NOT DONE"".",26,Findings,Perm,(ND),OE,
Record Qualifier,OE,OEREASND,Reason Not Done,Char,REASND,Reason not done. Used in conjunction with OESTAT when value is "NOT DONE".,27,Findings,Perm,,OE,
Record Qualifier,OE,OEXFN,External File Path,Char,XFN,"Filename for an external file, such as one for a retinal OCT image.",28,Findings,Perm,,OE,
Record Qualifier,OE,OELOC,Location Used for the Measurement,Char,LOC,"Anatomical location of the subject relevant to the collection of the measurement. Examples: ""EYE"" for a finding record relative to the complete eye, ""RETINA"" for a measurement or assessment of only the retina.",29,Findings,Exp,(LOC),OE,
Variable Qualifier,OE,OELAT,Laterality,Char,LAT,"Qualifier for anatomical location or specimen further detailing laterality. Examples: ""RIGHT"", ""LEFT"", ""BILATERAL"".",30,Findings,Exp,(LAT),OE,
Variable Qualifier,OE,OEDIR,Directionality,Char,DIR,"Qualifier for anatomical location or specimen further detailing directionality. Examples: ""ANTERIOR"", ""LOWER"", ""PROXIMAL"".",31,Findings,Perm,(DIR),OE,
Variable Qualifier,OE,OEPORTOT,Portion or Totality,Char,PORTOT,"Qualifier for anatomical location or specimen further detailing the distribution, which means arrangement of, apportioning of. Examples: ""ENTIRE"", ""SINGLE"", ""SEGMENT"", ""MANY"".",32,Findings,Perm,(PORTOT),OE,
Record Qualifier,OE,OEMETHOD,Method of Test or Examination,Char,METHOD,"Method of the test or examination. Example: ""ETDRS EYE CHART"" for OETESTCD = ""NUMLCOR"". The different methods may offer different functionality or granularity, affecting the set of results and associated meaning.",33,Findings,Exp,(METHOD),OE,
Record Qualifier,OE,OELOBXFL,Last Observation Before Exposure Flag,Char,LOBXFL,Operationally-derived indicator used to identify the last non-missing value prior to RFXSTDTC. The value should be "Y" or null.,34,Findings,Exp,(NY),OE,
Record Qualifier,OE,OEBLFL,Baseline Flag,Char,BLFL,Indicator used to identify a baseline value. Should be "Y" or null. Note that OEBLFL is retained for backward compatibility. The authoritative baseline for statistical analysis is in an ADaM dataset.,35,Findings,Perm,(NY),OE,
Record Qualifier,OE,OEDRVFL,Derived Flag,Char,DRVFL,"Used to indicate a derived record (e.g., a record that represents the average of other records such as a computed baseline). Should be ""Y"" or null.",36,Findings,Perm,(NY),OE,
Record Qualifier,OE,OEEVAL,Evaluator,Char,EVAL,"Role of the person who provided the evaluation. Used only for results that are subjective (e.g., assigned by a person or a group). Examples: ""INDEPENDENT ASSESSOR"", ""INVESTIGATOR"".",37,Findings,Perm,(EVAL),OE,
Variable Qualifier,OE,OEEVALID,Evaluator Identifier,Char,EVALID,Used to distinguish multiple evaluators with the same role recorded in OEEVAL. Examples: "RADIOLOGIST1" or "RADIOLOGIST2".,38,Findings,Perm,(MEDEVAL),OE,
Record Qualifier,OE,OEACPTFL,Accepted Record Flag,Char,ACPTFL,"In cases where more than one assessor provides an evaluation of a result or response, this flag identifies the record that is considered, by an independent assessor, to be the accepted evaluation. Expected to be ""Y"" or null.",39,Findings,Perm,(NY),OE,
Record Qualifier,OE,OEREPNUM,Repetition Number,Num,REPNUM,"The incidence number of a test that is repeated within a given timeframe for the same test. The level of granularity can vary, e.g., within a time point or within a visit. For example, multiple measurements of blood pressure or multiple analyses of a sample.",40,Findings,Perm,,OE,
Timing,OE,VISITNUM,Visit Number,Num,VISITNUM,"Clinical encounter number. Numeric version of VISIT, used for sorting.",41,Findings,Exp,,,
Timing,OE,VISIT,Visit Name,Char,VISIT,Protocol-defined description of a clinical encounter.,42,Findings,Perm,,,
Timing,OE,VISITDY,Planned Study Day of Visit,Num,VISITDY,Planned study day of the visit based upon RFSTDTC in Demographics.,43,Findings,Perm,,,
Timing,OE,TAETORD,Planned Order of Element within Arm,Num,TAETORD,Number that gives the planned order of the Element within the Arm for the Element in which the assessment was made.,44,Findings,Perm,,,
Timing,OE,EPOCH,Epoch,Char,EPOCH,Epoch associated with the date/time at which the assessment was made.,45,Findings,Perm,(EPOCH),,
Timing,OE,OEDTC,Date/Time of Collection,Char,DTC,Collection date/time of the observation.,46,Findings,Exp,ISO 8601,OE,
Timing,OE,OEDY,Study Day of Visit/Collection/Exam,Num,DY,Actual study day of observation/exam expressed in integer days relative to the sponsor-defined RFSTDTC in Demographics.,47,Findings,Exp,,OE,
Timing,OE,OETPT,Planned Time Point Name,Char,TPT,Text description of time when a measurement or observation should be taken as defined in the protocol. This may be represented as an elapsed time relative to a fixed reference point.,48,Findings,Perm,,OE,
Timing,OE,OETPTNUM,Planned Time Point Number,Num,TPTNUM,Numeric version of planned time point used in sorting.,49,Findings,Perm,,OE,
Timing,OE,OEELTM,Planned Elapsed Time from Time Point Ref,Char,ELTM,"Planned elapsed time relative to a planned fixed reference (OETPTREF) such as ""Previous Dose"" or ""Previous Meal"". This variable is useful where there are repetitive measures. Not a clock time or a date/time variable, but an interval, represented as ISO duration.",50,Findings,Perm,ISO 8601,OE,
Timing,OE,OETPTREF,Time Point Reference,Char,TPTREF,"Description of the fixed reference point referred to by OETPT, OETPTNUM, and OEELTM.",51,Findings,Perm,,OE,
Timing,OE,OERFTDTC,Date/Time of Reference Time Point,Char,RFTDTC,"Date/time of the reference time point, OETPTREF.",52,Findings,Perm,ISO 8601,OE,
Identifier,PC,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Findings,Req,,,
Identifier,PC,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Findings,Req,PC,,
Identifier,PC,USUBJID,Unique Subject Identifier,Char,USUBJID,Unique subject identifier within the submission.,3,Findings,Req,,,
Identifier,PC,PCSEQ,Sequence Number,Num,SEQ,Sequence number given to ensure uniqueness of subject records within a domain. May be any valid number.,4,Findings,Req,,PC,
Identifier,PC,PCGRPID,Group ID,Char,GRPID,Used to tie together a block of related records in a single domain to support relationships within the domain and between domains.,5,Findings,Perm,,PC,
Identifier,PC,PCREFID,Reference ID,Char,REFID,Internal or external specimen identifier.,6,Findings,Perm,,PC,
Identifier,PC,PCSPID,Sponsor-Defined Identifier,Char,SPID,Sponsor-defined reference number.,7,Findings,Perm,,PC,
Topic,PC,PCTESTCD,Pharmacokinetic Test Short Name,Char,TESTCD,"Short name of the analyte or specimen characteristic. It can be used as a column name when converting a dataset from a vertical to a horizontal format. The value in PCTESTCD cannot be longer than 8 characters, nor can it start with a number (e.g., &quot;1TEST&quot; is not valid). PCTESTCD cannot contain characters other than letters, numbers, or underscores. Examples: &quot;ASA&quot;, &quot;VOL&quot;, &quot;SPG&quot;.",8,Findings,Req,,PC,
Synonym Qualifier,PC,PCTEST,Pharmacokinetic Test Name,Char,TEST,"Name of the analyte or specimen characteristic. Note any test normally performed by a clinical laboratory is considered a lab test. The value in PCTEST cannot be longer than 40 characters. Examples: &quot;Acetylsalicylic Acid&quot;, &quot;Volume&quot;, &quot;Specific Gravity&quot;.",9,Findings,Req,,PC,
Grouping Qualifier,PC,PCCAT,Test Category,Char,CAT,"Used to define a category of related records. Examples: &quot;ANALYTE&quot;, &quot;SPECIMEN PROPERTY&quot;.",10,Findings,Perm,,PC,
Grouping Qualifier,PC,PCSCAT,Test Subcategory,Char,SCAT,A further categorization of a test category.,11,Findings,Perm,,PC,
Result Qualifier,PC,PCORRES,Result or Finding in Original Units,Char,ORRES,Result of the measurement or finding as originally received or collected.,12,Findings,Exp,,PC,
Variable Qualifier,PC,PCORRESU,Original Units,Char,ORRESU,Original units in which the data were collected. The unit for PCORRES. Example: &quot;mg/L&quot;.,13,Findings,Exp,(PKUNIT),PC,
Result Qualifier,PC,PCSTRESC,Character Result/Finding in Std Format,Char,STRESC,"Contains the result value for all findings, copied or derived from PCORRES in a standard format or standard units. PCSTRESC should store all results or findings in character format; if results are numeric, they should also be stored in numeric format in PCSTRESN. For example, if a test has results &quot;NONE&quot;, &quot;NEG&quot;, and &quot;NEGATIVE&quot; in PCORRES, and these results effectively have the same meaning, they could be represented in standard format in PCSTRESC as &quot;NEGATIVE&quot;. For other examples, see general assumptions.",14,Findings,Exp,,PC,
Result Qualifier,PC,PCSTRESN,Numeric Result/Finding in Standard Units,Num,STRESN,Used for continuous or numeric results or findings in standard format; copied in numeric format from PCSTRESC. PCSTRESN should store all numeric test results or findings.,15,Findings,Exp,,PC,
Variable Qualifier,PC,PCSTRESU,Standard Units,Char,STRESU,Standardized unit used for PCSTRESC and PCSTRESN.,16,Findings,Exp,(PKUNIT),PC,
Record Qualifier,PC,PCSTAT,Completion Status,Char,STAT,Used to indicate a result was not obtained. Should be null if a result exists in PCORRES.,17,Findings,Perm,(ND),PC,
Record Qualifier,PC,PCREASND,Reason Test Not Done,Char,REASND,"Describes why a result was not obtained, such as &quot;SPECIMEN LOST&quot;. Used in conjunction with PCSTAT when value is &quot;NOT DONE&quot;.",18,Findings,Perm,,PC,
Record Qualifier,PC,PCNAM,Vendor Name,Char,NAM,Name or identifier of the laboratory or vendor who provides the test results.,19,Findings,Exp,,PC,
Record Qualifier,PC,PCSPEC,Specimen Material Type,Char,SPEC,"Defines the type of specimen used for a measurement. Examples: &quot;SERUM&quot;, &quot;PLASMA&quot;, &quot;URINE&quot;.",20,Findings,Exp,(SPECTYPE),PC,
Record Qualifier,PC,PCSPCCND,Specimen Condition,Char,SPCCND,"Free or standardized text describing the condition of the specimen, e.g., &quot;HEMOLYZED&quot;, &quot;ICTERIC&quot;, &quot;LIPEMIC&quot;.",21,Findings,Perm,(SPECCOND),PC,
Record Qualifier,PC,PCMETHOD,Method of Test or Examination,Char,METHOD,"Method of the test or examination. Examples: &quot;HPLC/MS&quot;, &quot;ELISA&quot;. This should contain sufficient information and granularity to allow differentiation of various methods that might have been used within a study.",22,Findings,Perm,(METHOD),PC,
Record Qualifier,PC,PCFAST,Fasting Status,Char,FAST,Indicator used to identify fasting status.,23,Findings,Perm,(NY),PC,
Record Qualifier,PC,PCDRVFL,Derived Flag,Char,DRVFL,"Used to indicate a derived record. The value should be &quot;Y&quot; or null. Records that represent the average of other records, which do not come from the CRF, are examples of records that would be derived for the submission datasets. If PCDRVFL = &quot;Y&quot;, then PCORRES may be null with PCSTRESC, and PCSTRESN (if the result is numeric) having the derived value.",24,Findings,Perm,(NY),PC,
Variable Qualifier,PC,PCLLOQ,Lower Limit of Quantitation,Num,LLOQ,Indicates the lower limit of quantitation for an assay. Units should be those used in PCSTRESU.,25,Findings,Exp,,PC,
Variable Qualifier,PC,PCULOQ,Upper Limit of Quantitation,Num,ULOQ,Indicates the upper limit of quantitation for an assay. Units should be those used in PCSTRESU.,26,Findings,Perm,,PC,
Timing,PC,VISITNUM,Visit Number,Num,VISITNUM,"1. Clinical encounter number. \n 2. Numeric version of VISIT, used for sorting.",27,Findings,Exp,,,
Timing,PC,VISIT,Visit Name,Char,VISIT,Protocol-defined description of clinical encounter.May be used in addition to VISITNUM and/or VISITDY.,28,Findings,Perm,,,
Timing,PC,VISITDY,Planned Study Day of Visit,Num,VISITDY,Planned study day of the visit based upon RFSTDTC in Demographics.,29,Findings,Perm,,,
Timing,PC,TAETORD,Planned Order of Element within Arm,Num,TAETORD,Number that gives the planned order of the Element within the Arm.,30,Findings,Perm,,,
Timing,PC,EPOCH,Epoch,Char,EPOCH,"Epoch associated with the start date/time of the observation, or the date/time of collection if start date/time is not collected.",31,Findings,Perm,(EPOCH),,
Timing,PC,PCDTC,Date/Time of Specimen Collection,Char,DTC,"Date/time of specimen collection represented in ISO 8601 character format. If there is no end time, then this will be the collection time.",32,Findings,Exp,ISO 8601,PC,
Timing,PC,PCENDTC,End Date/Time of Specimen Collection,Char,ENDTC,"End date/time of specimen collection represented in ISO 8601 character format. If there is no end time, the collection time should be stored in PCDTC, and PCENDTC should be null.",33,Findings,Perm,ISO 8601,PC,
Timing,PC,PCDY,Actual Study Day of Specimen Collection,Num,DY,"Study day of specimen collection, measured as integer days.Algorithm for calculations must be relative to the sponsor-defined RFSTDTC variable in Demographics.",34,Findings,Perm,,PC,
Timing,PC,PCENDY,Study Day of End of Observation,Num,ENDY,Actual study day of end of observation expressed in integer days relative to the sponsor-defined RFSTDTC in Demographics.,35,Findings,Perm,,PC,
Timing,PC,PCTPT,Planned Time Point Name,Char,TPT,"Text description of time when specimen should be taken.This may be represented as an elapsed time relative to a fixed reference point, such as time of last dose. See PCTPTNUM and PCTPTREF. Examples: &quot;Start&quot;, &quot;5 min post&quot;.",36,Findings,Perm,,PC,
Timing,PC,PCTPTNUM,Planned Time Point Number,Num,TPTNUM,Numerical version of PCTPT to aid in sorting.,37,Findings,Perm,,PC,
Timing,PC,PCELTM,Planned Elapsed Time from Time Point Ref,Char,ELTM,Planned elapsed time (in ISO 8601) relative to a planned fixed reference (PCTPTREF) such as &quot;PREVIOUS DOSE&quot; or &quot;PREVIOUS MEAL&quot;. This variable is useful where there are repetitive measures. Not a clock time or a date time variable.,38,Findings,Perm,ISO 8601,PC,
Timing,PC,PCTPTREF,Time Point Reference,Char,TPTREF,"Name of the fixed reference point used as a basis for PCTPT, PCTPTNUM, and PCELTM. Example: &quot;Most Recent Dose&quot;.",39,Findings,Perm,,PC,
Timing,PC,PCRFTDTC,Date/Time of Reference Point,Char,RFTDTC,Date/time of the reference time point described by PCTPTREF.,40,Findings,Perm,ISO 8601,PC,
Timing,PC,PCEVLINT,Evaluation Interval,Char,EVLINT,Evaluation Interval associated with a PCTEST record represented in ISO 8601 character format. Example: &quot;-PT2H&quot; to represent an interval of 2 hours prior to a PCTPT.,41,Findings,Perm,ISO 8601,PC,
Identifier,PE,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Findings,Req,,,
Identifier,PE,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Findings,Req,PE,,
Identifier,PE,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product.,3,Findings,Req,,,
Identifier,PE,PESEQ,Sequence Number,Num,SEQ,Sequence number to ensure uniqueness of records within a dataset for a subject. May be any valid number.,4,Findings,Req,,PE,
Identifier,PE,PEGRPID,Group ID,Char,GRPID,Used to link together a block of related records in a single domain for a subject.,5,Findings,Perm,,PE,
Identifier,PE,PESPID,Sponsor-Defined Identifier,Char,SPID,Sponsor-defined reference number. Perhaps preprinted on the CRF as an explicit line identifier or defined in the sponsor's operational database. Example: Line number on a CRF.,6,Findings,Perm,,PE,
Topic,PE,PETESTCD,Body System Examined Short Name,Char,TESTCD,"Short name of a part of the body examined in a physical examination. It can be used as a column name when converting a dataset from a vertical to a horizontal format. The value in PETESTCD cannot be longer than 8 characters, nor can it start with a number (e.g., &quot;1TEST&quot; is not valid). PETESTCD cannot contain characters other than letters, numbers, or underscores. Examples: &quot;HEAD&quot;, &quot;ENT&quot;. If the results of the entire physical examination are represented in one record, value should be &quot;PHYSEXAM&quot;.",7,Findings,Req,,PE,
Synonym Qualifier,PE,PETEST,Body System Examined,Char,TEST,"Long name of a part of the body examined in a physical examination. The value in PETEST cannot be longer than 40 characters. Examples: &quot;Head&quot;, &quot;Ear/Nose/Throat&quot;. If the results of the entire physical examination are represented in one record, value should be &quot;Physical Examination&quot;.",8,Findings,Req,,PE,
Synonym Qualifier,PE,PEMODIFY,Modified Reported Term,Char,MODIFY,"If the value of PEORRES is modified for coding purposes, then the modified text is placed here.",9,Findings,Perm,,PE,
Grouping Qualifier,PE,PECAT,Category for Examination,Char,CAT,Used to define a category of topic-variable values. Examples: &quot;GENERAL&quot;.,10,Findings,Perm,,PE,
Grouping Qualifier,PE,PESCAT,Subcategory for Examination,Char,SCAT,Used to define a further categorization of --CAT values.,11,Findings,Perm,,PE,
Record Qualifier,PE,PEBODSYS,Body System or Organ Class,Char,BODSYS,"Body system or organ class (MedDRA SOC) that is involved for a finding from the standard hierarchy for dictionary-coded results (e.g., MedDRA).",12,Findings,Perm,,PE,
Result Qualifier,PE,PEORRES,Verbatim Examination Finding,Char,ORRES,"Text description of any abnormal findings. If the examination was completed and there were no abnormal findings, the value should be &quot;NORMAL&quot;. If the examination was not performed on a particular body system, or at the subject level, then the value should be null, and &quot;NOT DONE&quot; should appear in PESTAT.",13,Findings,Exp,,PE,
Variable Qualifier,PE,PEORRESU,Original Units,Char,ORRESU,Original units in which the data were collected. The unit for PEORRES.,14,Findings,Perm,(UNIT),PE,
Result Qualifier,PE,PESTRESC,Character Result/Finding in Std Format,Char,STRESC,"If there are findings for a body system, then either the dictionary preferred term (if findings are coded using a dictionary) or PEORRES (if findings are not encoded) should appear here. If PEORRES is null, PESTRESC must be null.",15,Findings,Exp,,PE,
Record Qualifier,PE,PESTAT,Completion Status,Char,STAT,Used to indicate exam not done. Must be null if a result exists in PEORRES/PESTRESC.,16,Findings,Perm,(ND),PE,
Record Qualifier,PE,PEREASND,Reason Not Examined,Char,REASND,Describes why an examination was not performed or why a body system was not examined. Example: &quot;SUBJECT REFUSED&quot;. Used in conjunction with PESTAT when value is &quot;NOT DONE&quot;.,17,Findings,Perm,,PE,
Record Qualifier,PE,PELOC,Location of Physical Exam Finding,Char,LOC,Anatomical location of the subject relevant to the collection of the measurement. Example: &quot;ARM&quot; for skin rash.,18,Findings,Perm,(LOC),PE,
Variable Qualifier,PE,PELAT,Laterality,Char,LAT,"Qualifier for anatomical location or specimen further detailing laterallity. Examples: &quot;RIGHT&quot;, &quot;LEFT&quot;, &quot;BILATERAL&quot;.",19,Findings,Perm,(LAT),PE,
Record Qualifier,PE,PEMETHOD,Method of Test or Examination,Char,METHOD,"Method of the test or examination. Examples: &quot;PALPATION&quot;, &quot;PERCUSSION&quot;.",20,Findings,Perm,(METHOD),PE,
Record Qualifier,PE,PELOBXFL,Last Observation Before Exposure Flag,Char,LOBXFL,Operationally-derived indicator used to identify the last non-missing value prior to RFXSTDTC. Should be &quot;Y&quot; or null.,21,Findings,Perm,(NY),PE,
Record Qualifier,PE,PEBLFL,Baseline Flag,Char,BLFL,"A baseline defined by the sponsor (could be derived in the same manner as PELOBXFL or ABLFL, but is not required to be). The value should be &quot;Y&quot; or null. Note that PEBLFL is retained for backward compatibility. The authoritative baseline flag for statistical analysis is in an ADaM dataset.",22,Findings,Perm,(NY),PE,
Record Qualifier,PE,PEEVAL,Evaluator,Char,EVAL,"Role of the person who provided the evaluation. Used only for results that are subjective (e.g., assigned by a person or a group). Example: &quot;INVESTIGATOR&quot;.",23,Findings,Perm,(EVAL),PE,
Timing,PE,VISITNUM,Visit Number,Num,VISITNUM,"1. Clinical encounter number. \n 2. Numeric version of VISIT, used for sorting.",24,Findings,Exp,,,
Timing,PE,VISIT,Visit Name,Char,VISIT,Protocol-defined description of a clinical encounter.May be used in addition to VISITNUM and/or VISITDY.,25,Findings,Perm,,,
Timing,PE,VISITDY,Planned Study Day of Visit,Num,VISITDY,Planned study day of VISIT. Should be an integer.,26,Findings,Perm,,,
Timing,PE,TAETORD,Planned Order of Element within Arm,Num,TAETORD,Number that gives the planned order of the Element within the Arm for the Element in which the assessment was made.,27,Findings,Perm,,,
Timing,PE,EPOCH,Epoch,Char,EPOCH,Epoch associated with the observation date/time of the physical exam finding.,28,Findings,Perm,(EPOCH),,
Timing,PE,PEDTC,Date/Time of Examination,Char,DTC,Date and time of the physical examination represented in ISO 8601 character format.,29,Findings,Exp,ISO 8601,PE,
Timing,PE,PEDY,Study Day of Examination,Num,DY,"Study day of physical exam, measured as integer days.Algorithm for calculations must be relative to the sponsor-defined RFSTDTC variable in Demographics.",30,Findings,Perm,,PE,
Identifier,PP,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Findings,Req,,,
Identifier,PP,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Findings,Req,PP,,
Identifier,PP,USUBJID,Unique Subject Identifier,Char,USUBJID,Unique subject identifier within the submission.,3,Findings,Req,,,
Identifier,PP,PPSEQ,Sequence Number,Num,SEQ,Sequence number given to ensure uniqueness of subject records within a domain. May be any valid number.,4,Findings,Req,,PP,
Identifier,PP,PPGRPID,Group ID,Char,GRPID,Used to tie together a block of related records in a single domain to support relationships within the domain and between domains.,5,Findings,Perm,,PP,
Topic,PP,PPTESTCD,Parameter Short Name,Char,TESTCD,"Short name of the pharmacokinetic parameter. It can be used as a column name when converting a dataset from a vertical to a horizontal format. The value in PPTESTCD cannot be longer than 8 characters, nor can it start with a number (e.g., ""1TEST"" is not valid). PPTESTCD cannot contain characters other than letters, numbers, or underscores. Examples: ""AUCALL"", ""TMAX"", ""CMAX"".",6,Findings,Req,(PKPARMCD),PP,
Synonym Qualifier,PP,PPTEST,Parameter Name,Char,TEST,"Name of the pharmacokinetic parameter. The value in PPTEST cannot be longer than 40 characters. Examples: ""AUC All"", ""Time of CMAX"", ""Max Conc"".",7,Findings,Req,(PKPARM),PP,
Grouping Qualifier,PP,PPCAT,Parameter Category,Char,CAT,"Used to define a category of related records. For PP, this should be the name of the analyte in PCTEST whose profile the parameter is associated with.",8,Findings,Exp,,PP,
Grouping Qualifier,PP,PPSCAT,Parameter Subcategory,Char,SCAT,"Categorization of the model type used to calculate the PK parameters. Examples: ""COMPARTMENTAL"", ""NON-COMPARTMENTAL"".",9,Findings,Perm,,PP,
Result Qualifier,PP,PPORRES,Result or Finding in Original Units,Char,ORRES,Result of the measurement or finding as originally received or collected.,10,Findings,Exp,,PP,
Variable Qualifier,PP,PPORRESU,Original Units,Char,ORRESU,Original units in which the data were collected. The unit for PPORRES. Example: "ng/L". See PP Assumption 3.,11,Findings,Exp,(PKUNIT) \n (PKUWG) \n (PKUWKG) \n (PKUDMG) \n (PKUDUG),PP,
Result Qualifier,PP,PPSTRESC,Character Result/Finding in Std Format,Char,STRESC,"Contains the result value for all findings, copied or derived from PPORRES in a standard format or standard units. PPSTRESC should store all results or findings in character format; if results are numeric, they should also be stored in numeric format in PPSTRESN.",12,Findings,Exp,,PP,
Result Qualifier,PP,PPSTRESN,Numeric Result/Finding in Standard Units,Num,STRESN,Used for continuous or numeric results or findings in standard format; copied in numeric format from PPSTRESC. PPSTRESN should store all numeric test results or findings.,13,Findings,Exp,,PP,
Variable Qualifier,PP,PPSTRESU,Standard Units,Char,STRESU,Standardized unit used for PPSTRESC and PPSTRESN. See PP Assumption 3 .,14,Findings,Exp,(PKUNIT) \n (PKUWG) \n (PKUWKG) \n (PKUDMG) \n (PKUDUG),PP,
Record Qualifier,PP,PPSTAT,Completion Status,Char,STAT,Used to indicate that a parameter was not calculated. Should be null if a result exists in PPORRES.,15,Findings,Perm,(ND),PP,
Record Qualifier,PP,PPREASND,Reason Parameter Not Calculated,Char,REASND,"Describes why a parameter was not calculated, such as ""INSUFFICIENT DATA"". Used in conjunction with PPSTAT when value is ""NOT DONE"".",16,Findings,Perm,,PP,
Record Qualifier,PP,PPSPEC,Specimen Material Type,Char,SPEC,"Defines the type of specimen used for a measurement. If multiple specimen types are used for a calculation (e.g., serum and urine for renal clearance), then this field should be left blank. Examples: ""SERUM"", ""PLASMA"", ""URINE"".",17,Findings,Exp,(SPECTYPE),PP,
Timing,PP,TAETORD,Planned Order of Element within Arm,Num,TAETORD,Number that gives the planned order of the Element within the Arm.,18,Findings,Perm,,,
Timing,PP,EPOCH,Epoch,Char,EPOCH,"Epoch associated with the start date/time of the observation, or the date/time of collection if start date/time is not collected.",19,Findings,Perm,(EPOCH),,
Timing,PP,PPDTC,Date/Time of Parameter Calculations,Char,DTC,Nominal date/time of parameter calculations.,20,Findings,Perm,ISO 8601,PP,
Timing,PP,PPDY,Study Day of Parameter Calculations,Num,DY,"Study day of the collection, in integer days. The algorithm for calculations must be relative to the sponsor-defined RFSTDTC variable in the Demographics (DM) domain.",21,Findings,Perm,,PP,
Timing,PP,PPRFTDTC,Date/Time of Reference Point,Char,RFTDTC,Date/time of the reference time point from the PC records used to calculate a parameter record. The values in PPRFTDTC should be the same as that in PCRFTDTC for related records.,22,Findings,Exp,ISO 8601,PP,
Timing,PP,PPSTINT,Planned Start of Assessment Interval,Char,STINT,The start of a planned evaluation or assessment interval relative to the Time Point Reference.,23,Findings,Perm,ISO 8601,PP,
Timing,PP,PPENINT,Planned End of Assessment Interval,Char,ENINT,The end of a planned evaluation or assessment interval relative to the Time Point Reference.,24,Findings,Perm,ISO 8601,PP,
Identifier,QS,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Findings,Req,,,
Identifier,QS,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Findings,Req,QS,,
Identifier,QS,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product.,3,Findings,Req,,,
Identifier,QS,QSSEQ,Sequence Number,Num,SEQ,Sequence number given to ensure uniqueness of subject records within a domain. May be any valid number.,4,Findings,Req,,QS,
Identifier,QS,QSGRPID,Group ID,Char,GRPID,Used to tie together a block of related records in a single domain for a subject.,5,Findings,Perm,,QS,
Identifier,QS,QSSPID,Sponsor-Defined Identifier,Char,SPID,Sponsor-defined reference number. Perhaps preprinted on the CRF as an explicit line identifier or defined in the sponsor's operational database. Example: Question number on a questionnaire.,6,Findings,Perm,,QS,
Topic,QS,QSTESTCD,Question Short Name,Char,TESTCD,"Topic variable for QS. Short name for the value in QSTEST, which can be used as a column name when converting the dataset from a vertical format to a horizontal format. The value in QSTESTCD cannot be longer than 8 characters, nor can it start with a number (e.g., &quot;1TEST&quot; is not valid). QSTESTCD cannot contain characters other than letters, numbers, or underscores. \n Controlled terminology for QSTESTCD is published in separate codelists for each questionnaire. See https://www.cdisc.org/standards/semantics/terminology for values for QSTESTCD. Examples: &quot;ADCCMD01&quot;, &quot;BPR0103&quot;.",7,Findings,Req,,QS,
Synonym Qualifier,QS,QSTEST,Question Name,Char,TEST,Verbatim name of the question or group of questions used to obtain the measurement or finding. The value in QSTEST cannot be longer than 40 characters. \n Controlled terminology for QSTEST is published in separate codelists for each questionnaire. See https://www.cdisc.org/standards/semantics/terminology for vaues for QSTEST. Example: &quot;BPR01 - Emotional Withdrawal&quot;.,8,Findings,Req,,QS,
Grouping Qualifier,QS,QSCAT,Category of Question,Char,CAT,"Used to specify the questionnaire in which the question identified by QSTEST and QSTESTCD was included. Examples: &quot;ADAS-COG&quot;, &quot;MDS-UPDRS&quot;.",9,Findings,Req,(QSCAT),QS,
Grouping Qualifier,QS,QSSCAT,Subcategory for Question,Char,SCAT,"A further categorization of the questions within the category. Examples: &quot;MENTAL HEALTH&quot; , &quot;DEPRESSION&quot;, &quot;WORD RECALL&quot;.",10,Findings,Perm,,QS,
Result Qualifier,QS,QSORRES,Finding in Original Units,Char,ORRES,"Finding as originally received or collected (e.g., &quot;RARELY&quot;, &quot;SOMETIMES&quot;). When sponsors apply codelist to indicate the code values are statistically meaningful standardized scores, which are defined by sponsors or by valid methodologies such as SF36 questionnaires, QSORRES will contain the decode format, and QSSTRESC and QSSTRESN may contain the standardized code values or scores.",11,Findings,Exp,,QS,
Variable Qualifier,QS,QSORRESU,Original Units,Char,ORRESU,"Original units in which the data were collected. The unit for QSORRES, such as minutes or seconds or the units associated with a visual analog scale.",12,Findings,Perm,(UNIT),QS,
Result Qualifier,QS,QSSTRESC,Character Result/Finding in Std Format,Char,STRESC,"Contains the finding for all questions or sub-scores, copied or derived from QSORRES in a standard format or standard units. QSSTRESC should store all findings in character format; if findings are numeric, they should also be stored in numeric format in QSSTRESN. If question scores are derived from the original finding, then the standard format is the score. Examples: &quot;0&quot;, &quot;1&quot;. When sponsors apply codelist to indicate the code values are statistically meaningful standardized scores, which are defined by sponsors or by valid methodologies such as SF36 questionnaires, QSORRES will contain the decode format, and QSSTRESC and QSSTRESN may contain the standardized code values or scores.",13,Findings,Exp,,QS,
Result Qualifier,QS,QSSTRESN,Numeric Finding in Standard Units,Num,STRESN,Used for continuous or numeric findings in standard format; copied in numeric format from QSSTRESC. QSSTRESN should store all numeric results or findings.,14,Findings,Perm,,QS,
Variable Qualifier,QS,QSSTRESU,Standard Units,Char,STRESU,Standardized unit used for QSSTRESC or QSSTRESN.,15,Findings,Perm,(UNIT),QS,
Record Qualifier,QS,QSSTAT,Completion Status,Char,STAT,Used to indicate that a question was not done or was not answered. Should be null if a result exists in QSORRES.,16,Findings,Perm,(ND),QS,
Record Qualifier,QS,QSREASND,Reason Not Performed,Char,REASND,Describes why a question was not answered. Used in conjunction with QSSTAT when value is &quot;NOT DONE&quot;. Example: &quot;SUBJECT REFUSED&quot;.,17,Findings,Perm,,QS,
Record Qualifier,QS,QSLOBXFL,Last Observation Before Exposure Flag,Char,LOBXFL,Operationally-derived indicator used to identify the last non-missing value prior to RFXSTDTC. Should be &quot;Y&quot; or null.,18,Findings,Perm,(NY),QS,
Record Qualifier,QS,QSBLFL,Baseline Flag,Char,BLFL,Indicator used to identify a baseline value. Should be &quot;Y&quot; or null. Note that QSBLFL is retained for backward compatibility. The authoritative baseline for statistical analysis is in an ADaM dataset.,19,Findings,Perm,(NY),QS,
Record Qualifier,QS,QSDRVFL,Derived Flag,Char,DRVFL,"Used to indicate a derived record. The value should be &quot;Y&quot; or null. Records that represent the average of other records or questionnaire sub-scores that do not come from the CRF are examples of records that would be derived for the submission datasets. If QSDRVFL = &quot;Y&quot;, then QSORRES may be null with QSSTRESC and (if numeric) QSSTRESN having the derived value.",20,Findings,Perm,(NY),QS,
Record Qualifier,QS,QSEVAL,Evaluator,Char,EVAL,"Role of the person who provided the evaluation. Examples: &quot;STUDY SUBJECT&quot;, &quot;CAREGIVER&quot;, &quot;INVESTIGATOR&quot;.",21,Findings,Perm,(EVAL),QS,
Timing,QS,VISITNUM,Visit Number,Num,VISITNUM,"1. Clinical encounter number. \n 2. Numeric version of VISIT, used for sorting.",22,Findings,Exp,,,
Timing,QS,VISIT,Visit Name,Char,VISIT,Protocol-defined description of clinical encounter.May be used in addition to VISITNUM and/or VISITDY.,23,Findings,Perm,,,
Timing,QS,VISITDY,Planned Study Day of Visit,Num,VISITDY,Planned study day of the visit based upon RFSTDTC in Demographics.,24,Findings,Perm,,,
Timing,QS,TAETORD,Planned Order of Element within Arm,Num,TAETORD,Number that gives the planned order of the Element within the Arm for the Element in which the assessment was made.,25,Findings,Perm,,,
Timing,QS,EPOCH,Epoch,Char,EPOCH,Epoch associated with the observation date/time of the physical exam finding.,26,Findings,Perm,(EPOCH),,
Timing,QS,QSDTC,Date/Time of Finding,Char,DTC,Date of questionnaire.,27,Findings,Exp,ISO 8601,QS,
Timing,QS,QSDY,Study Day of Finding,Num,DY,"Study day of finding collection, measured as integer days.Algorithm for calculations must be relative to the sponsor-defined RFSTDTC variable in Demographics.",28,Findings,Perm,,QS,
Timing,QS,QSTPT,Planned Time Point Name,Char,TPT,"Text description of time when questionnaire should be administered.This may be represented as an elapsed time relative to a fixed reference point, such as time of last dose. See QSTPTNUM and QSTPTREF.",29,Findings,Perm,,QS,
Timing,QS,QSTPTNUM,Planned Time Point Number,Num,TPTNUM,Numerical version of QSTPT to aid in sorting.,30,Findings,Perm,,QS,
Timing,QS,QSELTM,Planned Elapsed Time from Time Point Ref,Char,ELTM,"Planned elapsed time (in ISO 8601) relative to a planned fixed reference (QSTPTREF). This variable is useful where there are repetitive measures. Not a clock time or a date time variable. Represented as an ISO 8601 duration. Examples: &quot;-PT15M&quot; to represent the period of 15 minutes prior to the reference point indicated by QSTPTREF, or &quot;PT8H&quot; to represent the period of 8 hours after the reference point indicated by QSTPTREF.",31,Findings,Perm,ISO 8601,QS,
Timing,QS,QSTPTREF,Time Point Reference,Char,TPTREF,"Name of the fixed reference point referred to by QSELTM, QSTPTNUM, and QSTPT. Examples: &quot;PREVIOUS DOSE&quot;, &quot;PREVIOUS MEAL&quot;.",32,Findings,Perm,,QS,
Timing,QS,QSRFTDTC,Date/Time of Reference Time Point,Char,RFTDTC,"Date/time of the reference time point, QSTPTREF.",33,Findings,Perm,ISO 8601,QS,
Timing,QS,QSEVLINT,Evaluation Interval,Char,EVLINT,Evaluation interval associated with a QSTEST question represented in ISO 8601 character format. Example: &quot;-P2Y&quot; to represent an interval of 2 years in the question &quot;Have you experienced any episodes in the past 2 years?&quot;.,34,Findings,Perm,ISO 8601,QS,
Identifier,RE,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Findings,Req,,,
Identifier,RE,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Findings,Req,RE,,
Identifier,RE,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product.,3,Findings,Req,,,
Identifier,RE,SPDEVID,Sponsor Device Identifier,Char,SPDEVID,Sponsor-defined identifier for a device.,4,Findings,Perm,,,
Identifier,RE,RESEQ,Sequence Number,Num,SEQ,Sequence number to ensure uniqueness of records within a dataset for a subject. May be any valid number (including decimals) and does not have to start at 1.,5,Findings,Req,,RE,
Identifier,RE,REGRPID,Group ID,Char,GRPID,"Optional group identifier, used to link together a block of related records within a subject in a domain.",6,Findings,Perm,,RE,
Identifier,RE,REREFID,Reference ID,Char,REFID,Optional internal or external procedure identifier.,7,Findings,Perm,,RE,
Identifier,RE,RESPID,Sponsor-Defined Identifier,Char,SPID,Sponsor-defined identifier. Perhaps preprinted on the CRF as an explicit line identifier or defined in the sponsor's operational database.,8,Findings,Perm,,RE,
Identifier,RE,RELNKID,Link ID,Char,LNKID,Identifier used to link related records across domains. This may be a one-to-one or a one-to-many relationship.,9,Findings,Perm,,RE,
Identifier,RE,RELNKGRP,Link Group,Char,LNKGRP,Identifier used to link related records across domains. This will usually be a many-to-one relationship.,10,Findings,Perm,,RE,
Topic,RE,RETESTCD,Short Name of Respiratory Test,Char,TESTCD,"Short name of the measurement, test, or examination. It can be used as a column name when converting a dataset from a vertical format to a horizontal format. The value in RETESTCD cannot be longer than 8 characters, nor can it start with a number (e.g., ""1TEST"" is not valid). RETESTCD cannot contain characters other than letters, numbers, or underscores. Examples: ""FEV1"", ""FVC"".",11,Findings,Req,(RETESTCD),RE,
Synonym Qualifier,RE,RETEST,Name of Respiratory Test,Char,TEST,"Verbatim name of the test or examination used to obtain the measurement or finding. The value in RETEST cannot be longer than 40 characters. Examples: ""Forced Expiratory Volume in 1 Second"", ""Forced Vital Capacity"".",12,Findings,Req,(RETEST),RE,
Grouping Qualifier,RE,RECAT,Category for Respiratory Test,Char,CAT,Used to categorize observations across subjects.,13,Findings,Perm,,RE,
Grouping Qualifier,RE,RESCAT,Subcategory for Respiratory Test,Char,SCAT,A further categorization.,14,Findings,Perm,,RE,
Record Qualifier,RE,REPOS,Position of Subject During Observation,Char,POS,"Position of the subject during a measurement or examination. Examples: ""SUPINE"", ""STANDING"", ""SITTING"".",15,Findings,Perm,(POSITION),RE,
Result Qualifier,RE,REORRES,Result or Finding in Original Units,Char,ORRES,Result of the procedure measurement or finding as originally received or collected.,16,Findings,Exp,,RE,
Variable Qualifier,RE,REORRESU,Original Units,Char,ORRESU,Original units in which the data were collected. The unit for REORRES and REORREF.,17,Findings,Perm,(UNIT),RE,
Variable Qualifier,RE,REORREF,Reference Result in Original Units,Char,ORREF,Reference result for continuous measurements in original units. Should be collected only for continuous results.,18,Findings,Perm,,RE,
Result Qualifier,RE,RESTRESC,Character Result/Finding in Std Format,Char,STRESC,"Contains the result value for all findings, copied or derived from REORRES in a standard format or in standard units. RESTRESC should store all results or findings in character format; if results are numeric, they should also be stored in numeric format in RESTRESN.",19,Findings,Exp,,RE,
Result Qualifier,RE,RESTRESN,Numeric Result/Finding in Standard Units,Num,STRESN,Used for continuous or numeric results or findings in standard format; copied in numeric format from RESTRESC. RESTRESN should store all numeric test results or findings.,20,Findings,Perm,,RE,
Variable Qualifier,RE,RESTRESU,Standard Units,Char,STRESU,"Standardized unit used for RESTRESC, RESTRESN and RESTREFN.",21,Findings,Perm,(UNIT),RE,
Variable Qualifier,RE,RESTREFC,Character Reference Result,Char,STREFC,Reference value for the result or finding copied or derived from --ORREF in a standard format.,22,Findings,Perm,,RE,
Variable Qualifier,RE,RESTREFN,Numeric Reference Result in Std Units,Num,STREFN,Reference result for continuous measurements in standard units. Should be populated only for continuous results.,23,Findings,Perm,,RE,
Record Qualifier,RE,RESTAT,Completion Status,Char,STAT,Used to indicate that a test was not done or a measurement was not taken. Should be null if a result exists in REORRES.,24,Findings,Perm,(ND),RE,
Record Qualifier,RE,REREASND,Reason Not Done,Char,REASND,"Describes why a measurement or test was not performed. Examples: ""BROKEN EQUIPMENT"", ""SUBJECT REFUSED"". Used in conjunction with RESTAT when value is ""NOT DONE"".",25,Findings,Perm,,RE,
Record Qualifier,RE,RELOC,Location Used for the Measurement,Char,LOC,"Anatomical location of the subject relevant to the collection of the measurement. Examples: ""LUNG"", ""BRONCHUS"".",26,Findings,Perm,(LOC),RE,
Variable Qualifier,RE,RELAT,Laterality,Char,LAT,"Side of the body used to collect measurement. Examples: ""RIGHT"", ""LEFT"".",27,Findings,Perm,(LAT),RE,
Variable Qualifier,RE,REDIR,Directionality,Char,DIR,"Qualifier for anatomical location or specimen further detailing directionality. Examples: ""ANTERIOR"", ""LOWER"", ""PROXIMAL"".",28,Findings,Perm,(DIR),RE,
Record Qualifier,RE,REMETHOD,Method of Test or Examination,Char,METHOD,Method used to create the result.,29,Findings,Perm,(METHOD),RE,
Record Qualifier,RE,RELOBXFL,Last Observation Before Exposure Flag,Char,LOBXFL,Operationally-derived indicator used to identify the last non-missing value prior to RFXSTDTC. The value should be "Y" or null.,30,Findings,Exp,(NY),RE,
Record Qualifier,RE,REBLFL,Baseline Flag,Char,BLFL,Indicator used to identify a baseline value. Should be Y or null. Note that REBLFL is retained for backward compatibility. The authoritative baseline flag for statistical analysis is in an ADaM dataset.,31,Findings,Perm,(NY),RE,
Record Qualifier,RE,REDRVFL,Derived Flag,Char,DRVFL,"Used to indicate a derived record. Should be ""Y"" or null. Records that represent the average of other records, or that do not come from the CRF, or are not as originally collected or received are examples of records that would be derived for the submission datasets. If REDRVFL = ""Y"", then REORRES could be null, with RESTRESC and (if numeric) RESTRESN having the derived value.",32,Findings,Perm,(NY),RE,
Record Qualifier,RE,REEVAL,Evaluator,Char,EVAL,"Role of the person who provided the evaluation. Used only for results that are subjective (e.g., assigned by a person or a group). Examples: ""ADJUDICATION COMMITTEE"", ""INDEPENDENT ASSESSOR"", ""RADIOLOGIST"".",33,Findings,Perm,(EVAL),RE,
Variable Qualifier,RE,REEVALID,Evaluator Identifier,Char,EVALID,Used to distinguish multiple evaluators with the same role recorded in REEVAL. Examples: "RADIOLOGIST1" or "RADIOLOGIST2".,34,Findings,Perm,(MEDEVAL),RE,
Record Qualifier,RE,REREPNUM,Repetition Number,Num,REPNUM,"The instance number of a test that is repeated within a given time frame for the same test. The level of granularity can vary, e.g., within a time point or within a visit. For example, multiple measurements of pulmonary function.",35,Findings,Perm,,RE,
Timing,RE,VISITNUM,Visit Number,Num,VISITNUM,"Clinical encounter number. Numeric version of VISIT, used for sorting.",36,Findings,Exp,,,
Timing,RE,VISIT,Visit Name,Char,VISIT,Protocol-defined description of a clinical encounter. May be used in addition to VISITNUM and/or VISITDY.,37,Findings,Perm,,,
Timing,RE,VISITDY,Planned Study Day of Visit,Num,VISITDY,Planned study day of the visit based upon RFSTDTC in Demographics.,38,Findings,Perm,,,
Timing,RE,TAETORD,Planned Order of Element within Arm,Num,TAETORD,Number that gives the planned order of the Element within the Arm for the Element in which the assessment was made.,39,Findings,Perm,,,
Timing,RE,EPOCH,Epoch,Char,EPOCH,Epoch associated with the date/time at which the assessment was made.,40,Findings,Perm,(EPOCH),,
Timing,RE,REDTC,Date/Time of Collection,Char,DTC,Date/time of procedure or test.,41,Findings,Exp,ISO 8601,RE,
Timing,RE,REDY,Study Day of Visit/Collection/Exam,Num,DY,Actual study day of visit/collection/exam expressed in integer days relative to the sponsor-defined RFSTDTC in Demographics.,42,Findings,Perm,,RE,
Timing,RE,RETPT,Planned Time Point Name,Char,TPT,"Text description of time when a measurement or observation should be taken as defined in the protocol. This may be represented as an elapsed time relative to a fixed reference point, such as time of last dose. See RETPTNUM and RETPTREF. Examples: ""Start"", ""5 minutes post"".",43,Findings,Perm,,RE,
Timing,RE,RETPTNUM,Planned Time Point Number,Num,TPTNUM,Numeric version of RETPT to aid in sorting.,44,Findings,Perm,,RE,
Timing,RE,REELTM,Planned Elapsed Time from Time Point Ref,Char,ELTM,"Planned Elapsed time relative to a planned fixed reference (RETPTREF). Not a clock time or a date/time variable, but an interval, represented as ISO duration. Examples: ""-PT15M"" to represent 15 minutes prior to the reference time point indicated by RETPTREF, or ""PT8H"" to represent 8 hours after the reference time point represented by RETPTREF.",45,Findings,Perm,ISO 8601,RE,
Timing,RE,RETPTREF,Time Point Reference,Char,TPTREF,"Description of the fixed reference point referred to by REELTM, RETPTNUM, and RETPT. Examples: ""PREVIOUS DOSE"", ""PREVIOUS MEAL"".",46,Findings,Perm,,RE,
Timing,RE,RERFTDTC,Date/Time of Reference Time Point,Char,RFTDTC,Date/time for a fixed reference time point defined by RETPTREF.,47,Findings,Perm,ISO 8601,RE,
Identifier,RP,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Findings,Req,,,
Identifier,RP,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Findings,Req,RP,,
Identifier,RP,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product.,3,Findings,Req,,,
Identifier,RP,RPSEQ,Sequence Number,Num,SEQ,"Sequence number to ensure uniqueness of records within a dataset for a subject (or within a parameter, in the case of the Trial Summary domain). May be any valid number (including decimals) and does not have to start at 1.",4,Findings,Req,,RP,
Identifier,RP,RPGRPID,Group ID,Char,GRPID,"Optional group identifier, used to link together a block of related records within a subject in a domain. Also used to link together a block of related records in the Trial Summary dataset.",5,Findings,Perm,,RP,
Identifier,RP,RPREFID,Reference ID,Char,REFID,"Optional internal or external identifier such as lab specimen ID, or UUID for an ECG waveform or a medical image.",6,Findings,Perm,,RP,
Identifier,RP,RPSPID,Sponsor-Defined Identifier,Char,SPID,Sponsor-defined identifier. Example: pre-printed line identifier on a case report form.,7,Findings,Perm,,RP,
Identifier,RP,RPLNKID,Link ID,Char,LNKID,Identifier used to link related records across domains. This may be a one-to-one or a one-to-many relationship.,8,Findings,Perm,,RP,
Identifier,RP,RPLNKGRP,Link Group ID,Char,LNKGRP,Identifier used to link related records across domains. This will usually be a many-to-one relationship.,9,Findings,Perm,,RP,
Topic,RP,RPTESTCD,Short Name of Reproductive Test,Char,TESTCD,"Short character value for RPTEST used as a column name when converting a dataset from a vertical format to a horizontal format. The short value can be up to 8 characters. Examples: ""CHILDPOT"", ""BCMETHOD"", ""MENARAGE"".",10,Findings,Req,(RPTESTCD),RP,
Synonym Qualifier,RP,RPTEST,Name of Reproductive Test,Char,TEST,"Long name For RPTESTCD. Examples: ""Childbearing Potential"", ""Birth Control Method"", ""Menarche Age"".",11,Findings,Req,(RPTEST),RP,
Grouping Qualifier,RP,RPCAT,Category for Reproductive Test,Char,CAT,"Used to define a category of topic-variable values. Examples: ""No use case to date, but values would be relative to reproduction tests grouping"".",12,Findings,Perm,,RP,
Grouping Qualifier,RP,RPSCAT,Subcategory for Reproductive Test,Char,SCAT,"Used to define a further categorization of RPCAT values. Example: ""No use case to date, but values would be relative to reproduction tests grouping"".",13,Findings,Perm,,RP,
Result Qualifier,RP,RPORRES,Result or Finding in Original Units,Char,ORRES,"Result of the measurement or finding as originally received or collected. Examples: ""120"", ""<1"", ""POS"".",14,Findings,Exp,,RP,
Variable Qualifier,RP,RPORRESU,Original Units,Char,ORRESU,"Unit for RPORRES. Examples: ""in"", ""LB"", ""kg/L"".",15,Findings,Perm,(UNIT),RP,
Result Qualifier,RP,RPSTRESC,Character Result/Finding in Std Format,Char,STRESC,"Contains the result value for all findings, copied or derived from RPORRES in a standard format or in standard units. RPSTRESC should store all results or findings in character format; if results are numeric, they should also be stored in numeric format in RPSTRESN. For example, if various tests have results ""NONE"", ""NEG"", and ""NEGATIVE"" in RPORRES, and these results effectively have the same meaning, they could be represented in standard format in RPSTRESC as ""NEGATIVE"".",16,Findings,Exp,,RP,
Result Qualifier,RP,RPSTRESN,Numeric Result/Finding in Standard Units,Num,STRESN,Used for continuous or numeric results or findings in standard format; copied in numeric format from RPSTRESC. RPSTRESN should store all numeric test results or findings.,17,Findings,Perm,,RP,
Variable Qualifier,RP,RPSTRESU,Standard Units,Char,STRESU,Standardized units used for RPSTRESC and RPSTRESN. Example: "mol/L".,18,Findings,Perm,(UNIT),RP,
Record Qualifier,RP,RPSTAT,Completion Status,Char,STAT,"Used to indicate that a question was not asked or a test was not done, or a test was attempted but did not generate a result. Should be null or have a value of ""NOT DONE"".",19,Findings,Perm,(ND),RP,
Record Qualifier,RP,RPREASND,Reason Not Done,Char,REASND,Reason not done. Used in conjunction with RPSTAT when value is "NOT DONE".,20,Findings,Perm,,RP,
Record Qualifier,RP,RPLOBXFL,Last Observation Before Exposure Flag,Char,LOBXFL,Operationally-derived indicator used to identify the last non-missing value prior to RFXSTDTC. The value should be "Y" or null.,21,Findings,Perm,(NY),RP,
Record Qualifier,RP,RPBLFL,Baseline Flag,Char,BLFL,Indicator used to identify a baseline value. Should be "Y" or null. Note that RPBLFL is retained for backward compatibility. The authoritative baseline for statistical analysis is in an ADaM dataset.,22,Findings,Perm,(NY),RP,
Record Qualifier,RP,RPDRVFL,Derived Flag,Char,DRVFL,"Used to indicate a derived record. The value should be ""Y"" or null. Records which represent the average of other records or which do not come from the CRF are examples of records that would be derived for the submission datasets. If RPDRVFL = ""Y"", then RPORRES may be null, with RPSTRESC and (if numeric) RPSTRESN having the derived value.",23,Findings,Perm,(NY),RP,
Timing,RP,VISITNUM,Visit Number,Num,VISITNUM,"Clinical encounter number. Numeric version of VISIT, used for sorting.",24,Findings,Exp,,,
Timing,RP,VISIT,Visit Name,Char,VISIT,Protocol-defined description of a clinical encounter.,25,Findings,Perm,,,
Timing,RP,VISITDY,Planned Study Day of Visit,Num,VISITDY,Planned study day of VISIT. Should be an integer.,26,Findings,Perm,,,
Timing,RP,TAETORD,Planned Order of Element within Arm,Num,TAETORD,Number that gives the planned order of the Element within the Arm for the Element in which the assessment was made.,27,Findings,Perm,,,
Timing,RP,EPOCH,Epoch,Char,EPOCH,Epoch associated with the date/time at which the assessment was made.,28,Findings,Perm,(EPOCH),,
Timing,RP,RPDTC,Date/Time of Collection,Char,DTC,Collection date and time of an observation.,29,Findings,Exp,ISO 8601,RP,
Timing,RP,RPDY,Study Day of Visit/Collection/Exam,Num,DY,Actual study day of visit/collection/exam expressed in integer days relative to the sponsor-defined RFSTDTC in Demographics.,30,Findings,Perm,,RP,
Timing,RP,RPDUR,Duration,Char,DUR,"Collected duration of an event, intervention, or finding represented in ISO 8601 character format. Used only if collected on the CRF and not derived.",31,Findings,Perm,ISO 8601,RP,
Timing,RP,RPTPT,Planned Time Point Name,Char,TPT,"Text description of time when a measurement or observation should be taken as defined in the protocol. This may be represented as an elapsed time relative to a fixed reference point, such as time of last dose.",32,Findings,Perm,,RP,
Timing,RP,RPTPTNUM,Planned Time Point Number,Num,TPTNUM,Numeric version of planned time point used in sorting.,33,Findings,Perm,,RP,
Timing,RP,RPELTM,Planned Elapsed Time from Time Point Ref,Char,ELTM,"Planned elapsed time in ISO 8601 character format relative to a planned fixed reference (RPTPTREF) such as ""Previous Dose"" or ""Previous Meal"". This variable is useful where there are repetitive measures. Not a clock time or a date/time variable, but an interval, represented as ISO duration.",34,Findings,Perm,ISO 8601,RP,
Timing,RP,RPTPTREF,Time Point Reference,Char,TPTREF,"Description of the fixed reference point referred to by RPELTM, RPTPTNUM, and RPTPT. Examples: ""PREVIOUS DOSE"", ""PREVIOUS MEAL"".",35,Findings,Perm,,RP,
Timing,RP,RPRFTDTC,Date/Time of Reference Time Point,Char,RFTDTC,Date/time for a fixed reference time point defined by RPTPTREF in ISO 8601 character format.,36,Findings,Perm,ISO 8601,RP,
Identifier,RS,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Findings,Req,,,
Identifier,RS,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Findings,Req,RS,,
Identifier,RS,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product.,3,Findings,Req,,,
Identifier,RS,RSSEQ,Sequence Number,Num,SEQ,Sequence number given to ensure uniqueness within a dataset for a subject. May be any valid number.,4,Findings,Req,,RS,
Identifier,RS,RSGRPID,Group ID,Char,GRPID,Used to link together a block of related records within a subject in a domain.,5,Findings,Perm,,RS,
Identifier,RS,RSREFID,Reference ID,Char,REFID,Internal or external identifier.,6,Findings,Perm,,RS,
Identifier,RS,RSSPID,Sponsor-Defined Identifier,Char,SPID,Sponsor-defined identifier.,7,Findings,Perm,,RS,
Identifier,RS,RSLNKID,Link ID,Char,LNKID,An identifier used to link the response assessment to the related measurement record in another domain which was used to determine the response result. LNKID values group records within USUBJID.,8,Findings,Perm,,RS,
Identifier,RS,RSLNKGRP,Link Group ID,Char,LNKGRP,A grouping identifier used to link the response assessment to a group of measurement/assessment records which were used in the assessment of the response. LNKGRP values group records within USUBJID.,9,Findings,Perm,,RS,
Topic,RS,RSTESTCD,Assessment Short Name,Char,TESTCD,"Short name of the TEST in RSTEST. RSTESTCD cannot contain characters other than letters, numbers, or underscores. Examples: ""TRGRESP"", ""NTRGRESP"", ""OVRLRESP"", ""SYMPTDTR"", ""CPS0102"". \n There are separate codelists used for RSTESTCD where the choice depends on the value of RSCAT. Codelist ""ONCRTSCD"" is used for oncology response criteria (when RSCAT is a term in codelist ""ONCRSCAT""). Examples: TRGRESP, ""NTRGRESP, ""OVRLRESSP"". For Clinical Classifications (when RSCAT is a term in codelist ""CCCAT""), QRS Naming Rules apply. These instruments have individual dedicated terminology codelists.",10,Findings,Req,(ONCRTSCD),RS,
Synonym Qualifier,RS,RSTEST,Assessment Name,Char,TEST,"Verbatim name of the response assessment. The value in RSTEST cannot be longer than 40 characters. \n There are separate codelists used for RSTEST where the choice depends on the value of RSCAT. Codelist ""ONCRTS"" is used for oncology response criteria (when RSCAT is a term in codelist ""ONCRSCAT""). Examples: ""Target Response"", ""Non-target Response"", ""Overall Response"", ""Symptomatic Deterioration"", ""CPS01-Ascites"". For Clinical Classifications (when RSCAT is a term in codelist ""CCCAT""), QRS Naming Rules apply. These instruments have individual dedicated terminology codelists. For Clinical Classifications, QRS Naming Rules apply. These instruments have individual dedicated terminology codelists.",11,Findings,Req,(ONCRTS),RS,
Grouping Qualifier,RS,RSCAT,Category for Assessment,Char,CAT,"Used to define a category of related records across subjects. Examples: ""RECIST 1.1"", ""CHILD-PUGH CLASSIFICATION"". There are separate codelists used for RSCAT where the choice depends on whether the related records are about an oncology response criterion or another clinical classification. \n RSCAT is required for clinical classifications other than oncology response criteria.",12,Findings,Exp,(ONCRSCAT) \n (CCCAT),RS,
Grouping Qualifier,RS,RSSCAT,Subcategory,Char,SCAT,Used to define a further categorization of RSCAT values.,13,Findings,Perm,,RS,
Result Qualifier,RS,RSORRES,Result or Finding in Original Units,Char,ORRES,"Result of the response assessment as originally received, collected, or calculated.",14,Findings,Exp,,RS,
Variable Qualifier,RS,RSORRESU,Original Units,Char,ORRESU,Unit for RSORRES.,15,Findings,Perm,(UNIT),RS,
Result Qualifier,RS,RSSTRESC,Character Result/Finding in Std Format,Char,STRESC,"Contains the result value for the response assessment, copied, or derived from RSORRES in a standard format or standard units. RSSTRESC should store all results or findings in character format. \n For Clinical Classifications, this may be a score.",16,Findings,Exp,(ONCRSR),RS,
Result Qualifier,RS,RSSTRESN,Numeric Result/Finding in Standard Units,Num,STRESN,"Used for continuous or numeric results or findings in standard format; copied in numeric format from --STRESC. --STRESN should store all numeric test results or findings. For Clinical Classifications, this may be a score.",17,Findings,Perm,,RS,
Variable Qualifier,RS,RSSTRESU,Standard Units,Char,STRESU,Standardized units used for RSSTRESC and RSSTRESN.,18,Findings,Perm,(UNIT),RS,
Record Qualifier,RS,RSSTAT,Completion Status,Char,STAT,Used to indicate the response assessment was not performed. Should be null if a result exists in RSORRES.,19,Findings,Perm,(ND),RS,
Record Qualifier,RS,RSREASND,Reason Not Done,Char,REASND,"Describes why a response assessment was not performed. Examples: ""All target tumors not evaluated"", ""Subject does not have non-target tumors"". Used in conjunction with RSSTAT when value is ""NOT DONE"".",20,Findings,Perm,,RS,
Record Qualifier,RS,RSNAM,Vendor Name,Char,NAM,The name or identifier of the vendor that performed the response assessment. This column can be left null when the investigator provides the complete set of data in the domain.,21,Findings,Perm,,RS,
Record Qualifier,RS,RSLOBXFL,Last Observation Before Exposure Flag,Char,LOBXFL,"Operationally-derived indicator used to identify the last non-missing value prior to RFXSTDTC. The value should be ""Y"" or null. \n When a clinical classification is assessed at multiple times, including baseline, RSLOBXFL should be included in the dataset.",22,Findings,Perm,(NY),RS,
Record Qualifier,RS,RSBLFL,Baseline Flag,Char,BLFL,Indicator used to identify a baseline value. Should be "Y" or null. Note that --BLFL is retained for backward compatibility. The authoritative baseline for statistical analysis is in an ADaM dataset.,23,Findings,Perm,(NY),RS,
Record Qualifier,RS,RSDRVFL,Derived Flag,Char,DRVFL,"Used to indicate a derived record (e.g., a record that represents the average of other records such as a computed baseline). Should be ""Y"" or null.",24,Findings,Perm,(NY),RS,
Record Qualifier,RS,RSEVAL,Evaluator,Char,EVAL,"Role of the person who provided the evaluation. Used only for results that are subjective (e.g., assigned by a person or a group). Examples: ""ADJUDICATION COMMITTEE"", ""INDEPENDENT ASSESSOR"", ""RADIOLOGIST"". \n RSEVAL is expected for oncology response criteria. It can be left null when the investigator provides the complete set of data in the domain. However, the column should contain no null values when data from one or more independent assessors is included, meaning that the rows attributed to the investigator should contain a value of ""INVESTIGATOR"".",25,Findings,Perm,(EVAL),RS,
Variable Qualifier,RS,RSEVALID,Evaluator Identifier,Char,EVALID,"Used to distinguish multiple evaluators with the same role recorded in RSEVAL. Examples: ""RADIOLOGIST1"", ""RADIOLOGIST2"". See RS Assumption 9.",26,Findings,Perm,(MEDEVAL),RS,
Record Qualifier,RS,RSACPTFL,Accepted Record Flag,Char,ACPTFL,"In cases where more than one independent assessor (e.g., ""RADIOLOGIST 1"", ""RADIOLOGIST 2"", ""ADJUDICATOR"") provides an evaluation of response, this flag identifies the record that is considered to be the accepted evaluation.",27,Findings,Perm,(NY),RS,
Timing,RS,VISITNUM,Visit Number,Num,VISITNUM,"Clinical encounter number. Numeric version of VISIT, used for sorting.",28,Findings,Exp,,,
Timing,RS,VISIT,Visit Name,Char,VISIT,Protocol-defined description of a clinical encounter.,29,Findings,Perm,,,
Timing,RS,VISITDY,Planned Study Day of Visit,Num,VISITDY,Planned study day of the visit based upon RFSTDTC in Demographics.,30,Findings,Perm,,,
Timing,RS,TAETORD,Planned Order of Element within Arm,Num,TAETORD,Number that gives the planned order of the Element within the Arm for the Element in which the assessment was made.,31,Findings,Perm,,,
Timing,RS,EPOCH,Epoch,Char,EPOCH,Epoch associated with the date/time at which the assessment was made.,32,Findings,Perm,(EPOCH),,
Timing,RS,RSDTC,Date/Time of Assessment,Char,DTC,Collection date and time of the assessment represented in ISO 8601 character format.,33,Findings,Exp,ISO 8601,RS,
Timing,RS,RSDY,Study Day of Assessment,Num,DY,"Study day of the assessment, measured as integer days. Algorithm for calculations must be relative to the sponsor-defined RFSTDTC variable in Demographics.",34,Findings,Perm,,RS,
Timing,RS,RSTPT,Planned Time Point Name,Char,TPT,"Text description of time when a measurement or observation should be taken as defined in the protocol. This may be represented as an elapsed time relative to a fixed reference point, such as time of last dose. See RSTPTNUM and RSTPTREF.",35,Findings,Perm,,RS,
Timing,RS,RSTPTNUM,Planned Time Point Number,Num,TPTNUM,Numeric version of planned time point used in sorting.,36,Findings,Perm,,RS,
Timing,RS,RSELTM,Planned Elapsed Time from Time Point Ref,Char,ELTM,"Planned elapsed time in ISO 8601 character format relative to a planned fixed reference (RSTPTREF) such as ""Previous Dose"" or ""Previous Meal"". This variable is useful where there are repetitive measures. Not a clock time or a date/time variable, but an interval, represented as ISO duration.",37,Findings,Perm,ISO 8601,RS,
Timing,RS,RSTPTREF,Time Point Reference,Char,TPTREF,"Description of the fixed reference point referred to by RSELTM, RSTPTNUM, and RSTPT. Examples: ""PREVIOUS DOSE"", ""PREVIOUS MEAL"".",38,Findings,Perm,,RS,
Timing,RS,RSRFTDTC,Date/Time of Reference Time Point,Char,RFTDTC,Date/time for a fixed reference time point defined by RSTPTREF in ISO 8601 character format.,39,Findings,Perm,ISO 8601,RS,
Timing,RS,RSEVLINT,Evaluation Interval,Char,EVLINT,"Duration of interval associated with an observation such as a finding RSTESTCD, represented in ISO 8601 character format. Example: ""-P2M"" to represent a period of the past 2 months as the evaluation interval.",40,Findings,Perm,ISO 8601,RS,
Timing,RS,RSEVINTX,Evaluation Interval Text,Char,EVINTX,"Evaluation interval associated with an observation, where the interval is not able to be represented in ISO 8601 format. Examples: ""LIFETIME"", ""LAST NIGHT"", ""RECENTLY"", ""OVER THE LAST FEW WEEKS"".",41,Findings,Perm,,RS,
Timing,RS,RSSTRTPT,Start Relative to Reference Time Point,Char,STRTPT,"Identifies the start of the observation as being before or after the sponsor-defined reference time point defined by variable RSSTTPT. \n Not all values of the codelist are allowable for this variable. See Section 4.4.7, Use of Relative Timing Variables.",42,Findings,Perm,(STENRF),RS,
Timing,RS,RSSTTPT,Start Reference Time Point,Char,STTPT,Description or date/time in ISO 8601 character format of the sponsor-defined reference point referred to by RSSTRTPT. Examples: "2003-12-15" or "VISIT 1".,43,Findings,Perm,,RS,
Timing,RS,RSENRTPT,End Relative to Reference Time Point,Char,ENRTPT,"Identifies the end of the observation as being before or after the sponsor-defined reference time point defined by variable RSENTPT. \n Not all values of the codelist are allowable for this variable. See Section 4.4.7, Use of Relative Timing Variables.",44,Findings,Perm,(STENRF),RS,
Timing,RS,RSENTPT,End Reference Time Point,Char,ENTPT,Description or date/time in ISO 8601 character format of the sponsor-defined reference point referred to by RSENRTPT. Examples: "2003-12-25" or "VISIT 2".,45,Findings,Perm,,RS,
Identifier,SC,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Findings,Req,,,
Identifier,SC,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Findings,Req,SC,,
Identifier,SC,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product.,3,Findings,Req,,,
Identifier,SC,SCSEQ,Sequence Number,Num,SEQ,Sequence number given to ensure uniqueness of subject records within a domain. May be any valid number.,4,Findings,Req,,SC,
Identifier,SC,SCGRPID,Group ID,Char,GRPID,Used to tie together a block of related records in a single domain for a subject.,5,Findings,Perm,,SC,
Identifier,SC,SCSPID,Sponsor-Defined Identifier,Char,SPID,Sponsor-defined reference number. Perhaps preprinted on the CRF as an explicit line identifier or defined in the sponsor's operational database.,6,Findings,Perm,,SC,
Topic,SC,SCTESTCD,Subject Characteristic Short Name,Char,TESTCD,"Short name of the measurement, test, or examination described in SCTEST. It can be used as a column name when converting a dataset from a vertical to a horizontal format. The value in SCTESTCD cannot be longer than 8 characters, nor can it start with a number (e.g., &quot;1TEST&quot; is not valid). SCTESTCD cannot contain characters other than letters, numbers, or underscores. Example: &quot;MARISTAT&quot;, &quot;NATORIG&quot;.",7,Findings,Req,(SCTESTCD),SC,
Synonym Qualifier,SC,SCTEST,Subject Characteristic,Char,TEST,"Verbatim name of the test or examination used to obtain the measurement or finding. The value in SCTEST cannot be longer than 40 characters. Examples: &quot;Marital Status&quot;, &quot;National Origin&quot;.",8,Findings,Req,(SCTEST),SC,
Grouping Qualifier,SC,SCCAT,Category for Subject Characteristic,Char,CAT,Used to define a category of related records.,9,Findings,Perm,,SC,
Grouping Qualifier,SC,SCSCAT,Subcategory for Subject Characteristic,Char,SCAT,A further categorization of the subject characteristic.,10,Findings,Perm,,SC,
Result Qualifier,SC,SCORRES,Result or Finding in Original Units,Char,ORRES,Result of the subject characteristic as originally received or collected.,11,Findings,Exp,,SC,
Variable Qualifier,SC,SCORRESU,Original Units,Char,ORRESU,Original unit in which the data were collected. The unit for SCORRES.,12,Findings,Perm,(UNIT),SC,
Result Qualifier,SC,SCSTRESC,Character Result/Finding in Std Format,Char,STRESC,"Contains the result value for all findings, copied or derived from SCORRES in a standard format or standard units. SCSTRESC should store all results or findings in character format; if results are numeric, they should also be stored in numeric format in SCSTRESN. For example, if a test has results &quot;NONE&quot;, &quot;NEG&quot;, and &quot;NEGATIVE&quot; in SCORRES, and these results effectively have the same meaning, they could be represented in standard format in SCSTRESC as &quot;NEGATIVE&quot;.",13,Findings,Exp,,SC,
Result Qualifier,SC,SCSTRESN,Numeric Result/Finding in Standard Units,Num,STRESN,Used for continuous or numeric results or findings in standard format; copied in numeric format from SCSTRESC. SCSTRESN should store all numeric test results or findings.,14,Findings,Perm,,SC,
Variable Qualifier,SC,SCSTRESU,Standard Units,Char,STRESU,Standardized unit used for SCSTRESC or SCSTRESN.,15,Findings,Perm,(UNIT),SC,
Record Qualifier,SC,SCSTAT,Completion Status,Char,STAT,Used to indicate that the measurement was not done. Should be null if a result exists in SCORRES.,16,Findings,Perm,(ND),SC,
Record Qualifier,SC,SCREASND,Reason Not Performed,Char,REASND,Describes why the observation has no result. Example: &quot;Subject refused&quot;. Used in conjunction with SCSTAT when value is &quot;NOT DONE&quot;.,17,Findings,Perm,,SC,
Timing,SC,TAETORD,Planned Order of Element within Arm,Num,TAETORD,Number that gives the planned order of the Element within the Arm.,18,Findings,Perm,,,
Timing,SC,EPOCH,Epoch,Char,EPOCH,Epoch associated with the start date/time at which the assessment was made.,19,Findings,Perm,(EPOCH),,
Timing,SC,SCDTC,Date/Time of Collection,Char,DTC,Collection date and time of the subject characteristic represented in ISO 8601 character format.,20,Findings,Perm,ISO 8601,SC,
Timing,SC,SCDY,Study Day of Examination,Num,DY,"1. Study day of collection, measured as integer days. \n 2. Algorithm for calculations must be relative to the sponsor-defined RFSTDTC variable in Demographics.",21,Findings,Perm,,SC,
Identifier,SS,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Findings,Req,,,
Identifier,SS,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Findings,Req,SS,,
Identifier,SS,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product.,3,Findings,Req,,,
Identifier,SS,SSSEQ,Sequence Number,Num,SEQ,Sequence number given to ensure uniqueness of subject records within a domain. May be any valid number.,4,Findings,Req,,SS,
Identifier,SS,SSGRPID,Group ID,Char,GRPID,Used to tie together a block of related records in a single domain for a subject.,5,Findings,Perm,,SS,
Identifier,SS,SSSPID,Sponsor-Defined Identifier,Char,SPID,Sponsor-defined reference number. Perhaps preprinted on the CRF as an explicit line identifier or defined in the sponsor's operational database. Example: Line number from the procedure or test page.,6,Findings,Perm,,SS,
Topic,SS,SSTESTCD,Status Short Name,Char,TESTCD,"Short name of the status assessment described in SSTEST. It can be used as a column name when converting a dataset from a vertical to a horizontal format. The value in SSTESTCD cannot be longer than 8 characters, nor can it start with a number (e.g., &quot;1TEST&quot; is not valid). SSTESTCD cannot contain characters other than letters, numbers, or underscores. Example: &quot;SURVSTAT&quot;.",7,Findings,Req,(SSTESTCD),SS,
Synonym Qualifier,SS,SSTEST,Status Name,Char,TEST,Verbatim name of the status assessment used to obtain the finding. The value in SSTEST cannot be longer than 40 characters. Example: &quot;Survival Status&quot;.,8,Findings,Req,(SSTEST),SS,
Grouping Qualifier,SS,SSCAT,Category for Assessment,Char,CAT,Used to categorize observations across subjects.,9,Findings,Perm,,SS,
Grouping Qualifier,SS,SSSCAT,Subcategory for Assessment,Char,SCAT,A further categorization.,10,Findings,Perm,,SS,
Result Qualifier,SS,SSORRES,Result or Finding Original Result,Char,ORRES,Result of the status assessment finding as originally received or collected.,11,Findings,Exp,,SS,
Result Qualifier,SS,SSSTRESC,Character Result/Finding in Std Format,Char,STRESC,"Contains the result value for all findings, copied or derived from SSORRES in a standard format.",12,Findings,Exp,(SSTATRS),SS,
Record Qualifier,SS,SSSTAT,Completion Status,Char,STAT,Used to indicate a status assessment was not done. Should be null if a result exists in SSORRES.,13,Findings,Perm,(ND),SS,
Record Qualifier,SS,SSREASND,Reason Assessment Not Performed,Char,REASND,Describes why an assessment was not performed. Example: &quot;Subject Refused&quot;. Used in conjunction with SSSTAT when value is &quot;NOT DONE&quot;.,14,Findings,Perm,,SS,
Record Qualifier,SS,SSEVAL,Evaluator,Char,EVAL,"Role of the person who provided the evaluation. Used only for results that are subjective (e.g., assigned by a person or a group). Should be null for records that contain collected or derived data. Examples: &quot;CAREGIVER&quot;, &quot;ADJUDICATION COMMITTEE&quot;, &quot;FRIEND&quot;.",15,Findings,Perm,(EVAL),SS,
Timing,SS,VISITNUM,Visit Number,Num,VISITNUM,"1. Clinical encounter number. \n 2. Numeric version of VISIT, used for sorting.",16,Findings,Exp,,,
Timing,SS,VISIT,Visit Name,Char,VISIT,Protocol-defined description of clinical encounter.May be used in addition to VISITNUM and/or VISITDY.,17,Findings,Perm,,,
Timing,SS,VISITDY,Planned Study Day of Visit,Num,VISITDY,Planned study day of the visit based upon RFSTDTC in Demographics.,18,Findings,Perm,,,
Timing,SS,TAETORD,Planned Order of Element within Arm,Num,TAETORD,Number that gives the planned order of the Element within the Arm.,19,Findings,Perm,,,
Timing,SS,EPOCH,Epoch,Char,EPOCH,Epoch associated with the start date/time of the subject status assessment.,20,Findings,Perm,(EPOCH),,
Timing,SS,SSDTC,Date/Time of Assessment,Char,DTC,Date and time of the subject status assessment represented in ISO 8601 character format.,21,Findings,Exp,ISO 8601,SS,
Timing,SS,SSDY,Study Day of Assessment,Num,DY,"Study day of the test, measured as integer days.Algorithm for calculations must be relative to the sponsor-defined RFSTDTC variable in Demographics.",22,Findings,Perm,,SS,
Identifier,TR,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Findings,Req,,,
Identifier,TR,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Findings,Req,TR,,
Identifier,TR,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product.,3,Findings,Req,,,
Identifier,TR,TRSEQ,Sequence Number,Num,SEQ,Sequence number given to ensure uniqueness within a dataset for a subject. May be any valid number.,4,Findings,Req,,TR,
Identifier,TR,TRGRPID,Group ID,Char,GRPID,Used to link together a block of related records within a subject in a domain.,5,Findings,Perm,,TR,
Identifier,TR,TRREFID,Reference ID,Char,REFID,Internal or external identifier.,6,Findings,Perm,,TR,
Identifier,TR,TRSPID,Sponsor-Defined Identifier,Char,SPID,Sponsor-defined identifier.,7,Findings,Perm,,TR,
Identifier,TR,TRLNKID,Link ID,Char,LNKID,Identifier used to link the assessment result records to the individual tumor/lesion identification record in TU domain.,8,Findings,Exp,,TR,
Identifier,TR,TRLNKGRP,Link Group,Char,LNKGRP,Used to group and link all of the measurement/assessment records used in the assessment of the response record in the RS domain.,9,Findings,Perm,,TR,
Topic,TR,TRTESTCD,Tumor/Lesion Assessment Short Name,Char,TESTCD,"Short name of the TEST in TRTEST. TRTESTCD cannot contain characters other than letters, numbers, or underscores. Examples: ""TUMSTATE"", ""DIAMETER"", ""LESSCIND"", ""LESRVIND"". See TR Assumption 3.",10,Findings,Req,(TRTESTCD),TR,
Synonym Qualifier,TR,TRTEST,Tumor/Lesion Assessment Test Name,Char,TEST,"Verbatim name of the test or examination used to obtain the measurement or finding. The value in TRTEST cannot be longer than 40 characters. Examples: ""Tumor State"", ""Diameter"", ""Volume"", ""Lesion Success Indicator"", ""Lesion Revascularization Indicator"". See TR Assumption 3.",11,Findings,Req,(TRTEST),TR,
Result Qualifier,TR,TRORRES,Result or Finding in Original Units,Char,ORRES,Result of the tumor/lesion measurement/assessment as originally received or collected.,12,Findings,Exp,,TR,
Variable Qualifier,TR,TRORRESU,Original Units,Char,ORRESU,Original units in which the data were collected. The unit for TRORRES. Example: "mm".,13,Findings,Exp,(UNIT),TR,
Result Qualifier,TR,TRSTRESC,Character Result/Finding in Std Format,Char,STRESC,"Contains the result value for all findings, copied or derived from TRORRES in a standard format or standard units. TRSTRESC should store all results or findings in character format; if results are numeric, they should also be stored in numeric format in TRSTRESN.",14,Findings,Exp,(TRPROPRS),TR,
Result Qualifier,TR,TRSTRESN,Numeric Result/Finding in Standard Units,Num,STRESN,Used for continuous or numeric results or findings in standard format; copied in numeric format from TRSTRESC. TRSTRESN should store all numeric test results or findings.,15,Findings,Exp,,TR,
Variable Qualifier,TR,TRSTRESU,Standard Units,Char,STRESU,Standardized unit used for TRSTRESN.,16,Findings,Exp,(UNIT),TR,
Record Qualifier,TR,TRSTAT,Completion Status,Char,STAT,Used to indicate a scan/image/physical exam was not performed or a tumor/lesion measurement was not taken. Should be null if a result exists in TRORRES.,17,Findings,Perm,(ND),TR,
Record Qualifier,TR,TRREASND,Reason Not Done,Char,REASND,"Describes why a scan/image/physical exam was not performed or a tumor/lesion measurement was not taken. Examples: ""SCAN NOT PERFORMED"", ""NOT ASSESSABLE: IMAGE OBSCURED TUMOR"". Used in conjunction with TRSTAT when value is ""NOT DONE"".",18,Findings,Perm,,TR,
Record Qualifier,TR,TRNAM,Laboratory/Vendor Name,Char,NAM,The name or identifier of the vendor that performed the tumor/lesion measurement or assessment. This column can be left null when the investigator provides the complete set of data in the domain.,19,Findings,Perm,,TR,
Record Qualifier,TR,TRMETHOD,Method Used to Identify the Tumor/Lesion,Char,METHOD,"Method used to measure the tumor/lesion. Examples: ""MRI"", ""CT SCAN"", ""Coronary Angiography"".",20,Findings,Exp,(METHOD),TR,
Record Qualifier,TR,TRLOBXFL,Last Observation Before Exposure Flag,Char,LOBXFL,Operationally-derived indicator used to identify the last non-missing value prior to RFXSTDTC. Should be "Y" or null.,21,Findings,Exp,(NY),TR,
Record Qualifier,TR,TRBLFL,Baseline Flag,Char,BLFL,Indicator used to identify a baseline value. Should be "Y" or null. Note that TRBLFL is retained for backward compatibility. The authoritative baseline flag for statistical analysis is in an ADaM dataset.,22,Findings,Perm,(NY),TR,
Record Qualifier,TR,TREVAL,Evaluator,Char,EVAL,"Role of the person who provided the evaluation. Used only for results that are subjective (e.g., assigned by a person or a group). Examples: ""ADJUDICATION COMMITTEE"", ""INDEPENDENT ASSESSOR"".",23,Findings,Exp,(EVAL),TR,
Variable Qualifier,TR,TREVALID,Evaluator Identifier,Char,EVALID,"Used to distinguish multiple evaluators with the same role recorded in TREVAL. Examples:"" RADIOLOGIST1"", ""RADIOLOGIST2"". See TR Assumption 6.",24,Findings,Perm,(MEDEVAL),TR,
Record Qualifier,TR,TRACPTFL,Accepted Record Flag,Char,ACPTFL,"In cases where more than one independent assessor (e.g., ""RADIOLOGIST 1"", ""RADIOLOGIST 2"", ""ADJUDICATION COMMITTEE"") provide independent assessments at the same time point, this flag identifies the record that is considered to be the accepted assessment.",25,Findings,Perm,(NY),TR,
Timing,TR,VISITNUM,Visit Number,Num,VISITNUM,"Clinical encounter number. Numeric version of VISIT, used for sorting.",26,Findings,Exp,,,
Timing,TR,VISIT,Visit Name,Char,VISIT,Protocol-defined description of a clinical encounter.,27,Findings,Perm,,,
Timing,TR,VISITDY,Planned Study Day of Visit,Num,VISITDY,Planned study day of the visit based upon RFSTDTC in Demographics.,28,Findings,Perm,,,
Timing,TR,TAETORD,Planned Order of Element within Arm,Num,TAETORD,Epoch associated with the date/time at which the assessment was made.,29,Findings,Perm,,,
Timing,TR,EPOCH,Epoch,Char,EPOCH,Epoch associated with the Element in the planned sequence of Elements for the Arm to which the subject was assigned.,30,Findings,Perm,(EPOCH),,
Timing,TR,TRDTC,Date/Time of Tumor/Lesion Measurement,Char,DTC,The date of the scan/image/physical exam. TRDTC does not represent the date that the image was read to identify tumors/lesions. TRDTC also does not represent the VISIT date.,31,Findings,Exp,ISO 8601,TR,
Timing,TR,TRDY,Study Day of Tumor/Lesion Measurement,Num,DY,"Study day of the scan/image/physical exam, measured as integer days. Algorithm for calculations must be relative to the sponsor-defined RFSTDTC variable in Demographics.",32,Findings,Perm,,TR,
Identifier,TU,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Findings,Req,,,
Identifier,TU,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Findings,Req,TU,,
Identifier,TU,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product.,3,Findings,Req,,,
Identifier,TU,TUSEQ,Sequence Number,Num,SEQ,Sequence number given to ensure uniqueness within a dataset for a subject. May be any valid number.,4,Findings,Req,,TU,
Identifier,TU,TUGRPID,Group ID,Char,GRPID,Used to link together a block of related records within a subject in a domain. Can be used to group split or merged tumors/lesions which have been identified.,5,Findings,Perm,,TU,
Identifier,TU,TUREFID,Reference ID,Char,REFID,"Internal or external identifier, such as a medical image ID number.",6,Findings,Perm,,TU,
Identifier,TU,TUSPID,Sponsor-Defined Identifier,Char,SPID,Sponsor-defined identifier.,7,Findings,Perm,,TU,
Identifier,TU,TULNKID,Link ID,Char,LNKID,Identifier used to link identified tumor/lesion to the assessment results (in TR domain) over the course of the study.,8,Findings,Exp,,TU,
Identifier,TU,TULNKGRP,Link Group ID,Char,LNKGRP,Identifier used to link related records across domains. This will usually be a many-to-one relationship.,9,Findings,Perm,,TU,
Topic,TU,TUTESTCD,Tumor/Lesion ID Short Name,Char,TESTCD,"Short name of the TEST in TUTEST. TUTESTCD cannot be longer than 8 characters nor can start with a number. TUTESTCD cannot contain characters other than letters, numbers, or underscores. Example: ""TUMIDENT"". See TU Assumption 3.",10,Findings,Req,(TUTESTCD),TU,
Synonym Qualifier,TU,TUTEST,Tumor/Lesion ID Test Name,Char,TEST,Verbatim name of the test for the tumor/lesion identification. The value in TUTEST cannot be longer than 40 characters. Example: "Tumor Identification". See TU Assumption 3.,11,Findings,Req,(TUTEST),TU,
Result Qualifier,TU,TUORRES,Tumor/Lesion ID Result,Char,ORRES,"Result of the tumor/lesion identification. The result of tumor/lesion identification is a classification of the identified tumor/lesion. Examples: When TUTESTCD = ""TUMIDENT"", values of TUORRES might be ""TARGET"", ""NON-TARGET"", ""NEW"", or ""BENIGN ABNORMALITY"".",12,Findings,Exp,,TU,
Result Qualifier,TU,TUSTRESC,Tumor/Lesion ID Result Std. Format,Char,STRESC,Contains the result value for all findings copied or derived from TUORRES in a standard format.,13,Findings,Exp,(TUIDRS),TU,
Record Qualifier,TU,TUNAM,Laboratory/Vendor Name,Char,NAM,The name or identifier of the vendor that performed the tumor/lesion Identification. This column can be left null when the investigator provides the complete set of data in the domain.,14,Findings,Perm,,TU,
Record Qualifier,TU,TULOC,Location of the Tumor/Lesion,Char,LOC,"Used to specify the anatomical location of the identified tumor/lesion, e.g., ""LIVER"" \n Note: When anatomical location is broken down and collected as distinct pieces of data that when combined provide the overall location information (e.g., laterality/directionality/distribution), then the additional anatomical location qualifiers should be used. See Assumption 3.",15,Findings,Exp,(LOC),TU,
Variable Qualifier,TU,TULAT,Laterality,Char,LAT,"Qualifier for anatomical location or specimen further detailing laterality, for example, ""LEFT"", ""RIGHT"", ""BILATERAL"".",16,Findings,Perm,(LAT),TU,
Variable Qualifier,TU,TUDIR,Directionality,Char,DIR,"Qualifier for anatomical location or specimen further detailing directionality, for example, ""UPPER"", ""INTERIOR"".",17,Findings,Perm,(DIR),TU,
Variable Qualifier,TU,TUPORTOT,Portion or Totality,Char,PORTOT,"Qualifier for anatomical location or specimen further detailing the distribution, which means arrangement of, or apportioning of. Examples: ""ENTIRE"", ""SINGLE"", ""SEGMENT"", ""MULTIPLE"".",18,Findings,Perm,(PORTOT),TU,
Record Qualifier,TU,TUMETHOD,Method of Identification,Char,METHOD,"Method used to identify the tumor/lesion. Examples: ""MRI"", ""CT SCAN"".",19,Findings,Exp,(METHOD),TU,
Record Qualifier,TU,TULOBXFL,Last Observation Before Exposure Flag,Char,LOBXFL,Operationally-derived indicator used to identify the last non-missing value prior to RFXSTDTC. Should be "Y" or null.,20,Findings,Exp,(NY),TU,
Record Qualifier,TU,TUBLFL,Baseline Flag,Char,BLFL,Indicator used to identify a baseline value. Should be "Y" or null. Note that TUBLFL is retained for backward compatibility. The authoritative baseline flag for statistical analysis is in an ADaM dataset.,21,Findings,Perm,(NY),TU,
Record Qualifier,TU,TUEVAL,Evaluator,Char,EVAL,"Role of the person who provided the evaluation. Examples: ""ADJUDICATION COMMITTEE"", ""INDEPENDENT ASSESSOR"". \n This column can be left null when the investigator provides the complete set of data in the domain. However, the column should contain no null values when data from one or more independent assessors is included. For example, the rows attributed to the investigator should contain a value of ""INVESTIGATOR"".",22,Findings,Exp,(EVAL),TU,
Variable Qualifier,TU,TUEVALID,Evaluator Identifier,Char,EVALID,"Used to distinguish multiple evaluators with the same role recorded in --EVAL. Examples: ""RADIOLOGIST1"", ""RADIOLOGIST2"". See TU Assumption 8.",23,Findings,Perm,(MEDEVAL),TU,
Record Qualifier,TU,TUACPTFL,Accepted Record Flag,Char,ACPTFL,"In cases where more than one independent assessor (e.g., ""RADIOLOGIST 1"", ""RADIOLOGIST 2"", ""ADJUDICATION COMMITTEE"") provide independent assessments at the same time point, this flag identifies the record that is considered to be the accepted assessment.",24,Findings,Perm,(NY),TU,
Timing,TU,VISITNUM,Visit Number,Num,VISITNUM,"Clinical encounter number. Numeric version of VISIT, used for sorting.",25,Findings,Exp,,,
Timing,TU,VISIT,Visit Name,Char,VISIT,Protocol-defined description of a clinical encounter.,26,Findings,Perm,,,
Timing,TU,VISITDY,Planned Study Day of Visit,Num,VISITDY,Planned study day of the visit based upon RFSTDTC in Demographics. Should be an integer.,27,Findings,Perm,,,
Timing,TU,TAETORD,Planned Order of Element within Arm,Num,TAETORD,Number that gives the planned order of the Element within the Arm for the Element in which the assessment was made.,28,Findings,Perm,,,
Timing,TU,EPOCH,Epoch,Char,EPOCH,Epoch associated with the date/time at which the assessment was made.,29,Findings,Perm,(EPOCH),,
Timing,TU,TUDTC,Date/Time of Tumor/Lesion Identification,Char,DTC,TUDTC variable represents the date of the scan/image/physical exam. TUDTC does not represent the date that the image was read to identify tumors. TUDTC also does not represent the VISIT date.,30,Findings,Exp,ISO 8601,TU,
Timing,TU,TUDY,Study Day of Tumor/Lesion Identification,Num,DY,"Study day of the scan/image/physical exam, measured as integer days. Algorithm for calculations must be relative to the sponsor-defined RFSTDTC variable in Demographics.",31,Findings,Perm,,TU,
Identifier,UR,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Findings,Req,,,
Identifier,UR,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Findings,Req,UR,,
Identifier,UR,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product.,3,Findings,Req,,,
Identifier,UR,URSEQ,Sequence Number,Num,SEQ,Sequence number to ensure uniqueness of records within a dataset for a subject. May be any valid number (including decimals) and does not have to start at 1.,4,Findings,Req,,UR,
Identifier,UR,URGRPID,Group ID,Char,GRPID,"Optional group identifier, used to link together a block of related records within a subject in a domain.",5,Findings,Perm,,UR,
Identifier,UR,URREFID,Reference ID,Char,REFID,"Optional internal or external identifier such as lab specimen ID, or Universally Unique Identifier (UUID) for a medical image.",6,Findings,Perm,,UR,
Identifier,UR,URSPID,Sponsor-Defined Identifier,Char,SPID,Sponsor-defined identifier. Example: preprinted line identifier.,7,Findings,Perm,,UR,
Identifier,UR,URLNKID,Link ID,Char,LNKID,Identifier used to link related records across domains. This may be a one-to-one or a one-to-many relationship.,8,Findings,Perm,,UR,
Identifier,UR,URLNKGRP,Link Group ID,Char,LNKGRP,Identifier used to link related records across domains. This will usually be a many-to-one relationship.,9,Findings,Perm,,UR,
Topic,UR,URTESTCD,Short Name of Urinary Test,Char,TESTCD,"Short character value for URTEST used as a column name when converting a dataset from a vertical format to a horizontal format. It can be used as a column name when converting a dataset from a vertical to a horizontal format. The value in URTESTCD cannot be longer than 8 characters, nor can it start with a number (e.g., ""1TEST"" is not valid). URTESTCD cannot contain characters other than letters, numbers, or underscores. Examples: ""COUNT"", ""LENGTH"", ""RBLDFLW"".",10,Findings,Req,(URNSTSCD),UR,
Synonym Qualifier,UR,URTEST,Name of Urinary Test,Char,TEST,"Long name For URTESTCD. Examples: ""Count"", ""Length"", ""Renal Blood Flow"".",11,Findings,Req,(URNSTS),UR,
Variable Qualifier,UR,URTSTDTL,Urinary Test Detail,Char,TSTDTL,Further description of URTESTCD and URTEST.,12,Findings,Perm,,UR,
Grouping Qualifier,UR,URCAT,Category for Urinary Test,Char,CAT,Used to define a category of topic-variable values.,13,Findings,Perm,,UR,
Grouping Qualifier,UR,URSCAT,Subcategory for Urinary Test,Char,SCAT,Used to define a further categorization of URCAT values.,14,Findings,Perm,,UR,
Result Qualifier,UR,URORRES,Result or Finding in Original Units,Char,ORRES,Result of the measurement or finding as originally received or collected.,15,Findings,Exp,,UR,
Variable Qualifier,UR,URORRESU,Original Units,Char,ORRESU,Unit for URORRES.,16,Findings,Perm,(UNIT),UR,
Result Qualifier,UR,URSTRESC,Character Result/Finding in Std Format,Char,STRESC,"Contains the result value for all findings, copied or derived from URORRES in a standard format or in standard units. URSTRESC should store all results or findings in character format; if results are numeric, they should also be stored in numeric format in URSTRESN.",17,Findings,Exp,,UR,
Result Qualifier,UR,URSTRESN,Numeric Result/Finding in Standard Units,Num,STRESN,Used for continuous or numeric results or findings in standard format; copied in numeric format from URSTRESC. URSTRESN should store all numeric test results or findings.,18,Findings,Perm,,UR,
Variable Qualifier,UR,URSTRESU,Standard Units,Char,STRESU,Standardized units used for URSTRESC and URSTRESN.,19,Findings,Perm,(UNIT),UR,
Variable Qualifier,UR,URRESCAT,Result Category,Char,RESCAT,Used to categorize the result of a finding.,20,Findings,Perm,,UR,
Record Qualifier,UR,URSTAT,Completion Status,Char,STAT,"Used to indicate that a question was not asked or a test was not done, or a test was attempted but did not generate a result. Should be null or have a value of ""NOT DONE"".",21,Findings,Perm,(ND),UR,
Record Qualifier,UR,URREASND,Reason Not Done,Char,REASND,Reason not done. Used in conjunction with URSTAT when value is "NOT DONE".,22,Findings,Perm,,UR,
Record Qualifier,UR,URSPEC,Specimen Material Type,Char,SPEC,Defines the type of specimen used for a measurement.,23,Findings,Perm,(SPECTYPE),UR,
Record Qualifier,UR,URSPCUFL,Specimen Usability for the Test,Char,SPCUFL,"Describes the usability of the specimen for the test. The value will be ""N"" if the specimen is not usable, and null if the specimen is usable.",24,Findings,Perm,(NY),UR,
Record Qualifier,UR,URLOC,Location Used for the Measurement,Char,LOC,Anatomical location of the subject relevant to the collection of the measurement.,25,Findings,Perm,(LOC),UR,
Variable Qualifier,UR,URLAT,Laterality,Char,LAT,"Qualifier for anatomical location or specimen further detailing laterality. Examples: ""RIGHT"", ""LEFT"", ""BILATERAL"".",26,Findings,Perm,(LAT),UR,
Variable Qualifier,UR,URDIR,Directionality,Char,DIR,"Qualifier for anatomical location or specimen further detailing directionality. Examples: ""ANTERIOR"", ""LOWER"", ""PROXIMAL"".",27,Findings,Perm,(DIR),UR,
Record Qualifier,UR,URMETHOD,Method of Test or Examination,Char,METHOD,Method of the test or examination.,28,Findings,Perm,(METHOD),UR,
Record Qualifier,UR,URLOBXFL,Last Observation Before Exposure Flag,Char,LOBXFL,Operationally-derived indicator used to identify the last non-missing value prior to RFXSTDTC. The value should be "Y" or null.,29,Findings,Exp,(NY),UR,
Record Qualifier,UR,URBLFL,Baseline Flag,Char,BLFL,A baseline defined by the sponsor The value should be "Y" or null. Note that URBLFL is retained for backward compatibility. The authoritative baseline flag for statistical analysis is in an ADaM dataset.,30,Findings,Perm,(NY),UR,
Record Qualifier,UR,URDRVFL,Derived Flag,Char,DRVFL,"Used to indicate a derived record (e.g., a record that represents the average of other records such as a computed baseline). Should be ""Y"" or null.",31,Findings,Perm,(NY),UR,
Record Qualifier,UR,UREVAL,Evaluator,Char,EVAL,"Role of the person who provided the evaluation. Used only for results that are subjective (e.g., assigned by a person or a group). Examples: ""ADJUDICATION COMMITTEE"", ""INDEPENDENT ASSESSOR"", ""RADIOLOGIST"".",32,Findings,Perm,(EVAL),UR,
Variable Qualifier,UR,UREVALID,Evaluator Identifier,Char,EVALID,Used to distinguish multiple evaluators with the same role recorded in UREVAL. Examples: "RADIOLOGIST1" or "RADIOLOGIST2".,33,Findings,Perm,(MEDEVAL),UR,
Timing,UR,VISITNUM,Visit Number,Num,VISITNUM,"Clinical encounter number. Numeric version of VISIT, used for sorting.",34,Findings,Exp,,,
Timing,UR,VISIT,Visit Name,Char,VISIT,Protocol-defined description of a clinical encounter.,35,Findings,Perm,,,
Timing,UR,VISITDY,Planned Study Day of Visit,Num,VISITDY,Planned study day of VISIT. Should be an integer.,36,Findings,Perm,,,
Timing,UR,TAETORD,Planned Order of Element within Arm,Num,TAETORD,Number that gives the planned order of the Element within the Arm for the Element in which the observation was made.,37,Findings,Perm,,,
Timing,UR,EPOCH,Epoch,Char,EPOCH,Epoch associated with the date/time at which the observation was made.,38,Findings,Perm,(EPOCH),,
Timing,UR,URDTC,Date/Time of Collection,Char,DTC,Collection date and time of an observation.,39,Findings,Exp,ISO 8601,UR,
Timing,UR,URDY,Study Day of Visit/Collection/Exam,Num,DY,Actual study day of visit/collection/exam expressed in integer days relative to the sponsor-defined RFSTDTC in Demographics.,40,Findings,Perm,,UR,
Timing,UR,URTPT,Planned Time Point Name,Char,TPT,"Text description of time when a measurement or observation should be taken as defined in the protocol. This may be represented as an elapsed time relative to a fixed reference point, such as time of last dose. See URTPTNUM and URTPTREF.",41,Findings,Perm,,UR,
Timing,UR,URTPTNUM,Planned Time Point Number,Num,TPTNUM,Numeric version of planned time point used in sorting.,42,Findings,Perm,,UR,
Timing,UR,URELTM,Planned Elapsed Time from Time Point Ref,Char,ELTM,"Planned elapsed time relative to a planned fixed reference (URTPTREF) such as ""Previous Dose"" or ""Previous Meal"". This variable is useful where there are repetitive measures. Not a clock time or a date/time variable, but an interval, represented as ISO duration.",43,Findings,Perm,ISO 8601,UR,
Timing,UR,URTPTREF,Time Point Reference,Char,TPTREF,"Description of the fixed reference point referred to by URELTM, URTPTNUM, and URTPT. Examples: ""PREVIOUS DOSE"", ""PREVIOUS MEAL"".",44,Findings,Perm,,UR,
Timing,UR,URRFTDTC,Date/Time of Reference Time Point,Char,RFTDTC,Date/time for a fixed reference time point defined by URTPTREF.,45,Findings,Perm,ISO 8601,UR,
Identifier,VS,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Findings,Req,,,
Identifier,VS,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Findings,Req,VS,,
Identifier,VS,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product.,3,Findings,Req,,,
Identifier,VS,VSSEQ,Sequence Number,Num,SEQ,Sequence number given to ensure uniqueness of subject records within a domain. May be any valid number.,4,Findings,Req,,VS,
Identifier,VS,VSGRPID,Group ID,Char,GRPID,Used to tie together a block of related records in a single domain for a subject.,5,Findings,Perm,,VS,
Identifier,VS,VSSPID,Sponsor-Defined Identifier,Char,SPID,Sponsor-defined reference number. Perhaps pre-printed on the CRF as an explicit line identifier or defined in the sponsor's operational database.,6,Findings,Perm,,VS,
Topic,VS,VSTESTCD,Vital Signs Test Short Name,Char,TESTCD,"Short name of the measurement, test, or examination described in VSTEST. It can be used as a column name when converting a dataset from a vertical to a horizontal format. The value in VSTESTCD cannot be longer than 8 characters, nor can it start with a number (e.g., &quot;1TEST&quot; is not valid). VSTESTCD cannot contain characters other than letters, numbers, or underscores. Examples: &quot;SYSBP&quot;, &quot;DIABP&quot;, &quot;BMI&quot;.",7,Findings,Req,(VSTESTCD),VS,
Synonym Qualifier,VS,VSTEST,Vital Signs Test Name,Char,TEST,"Verbatim name of the test or examination used to obtain the measurement or finding. The value in VSTEST cannot be longer than 40 characters. Examples: &quot;Systolic Blood Pressure&quot;, &quot;Diastolic Blood Pressure&quot;, &quot;Body Mass Index&quot;.",8,Findings,Req,(VSTEST),VS,
Grouping Qualifier,VS,VSCAT,Category for Vital Signs,Char,CAT,Used to define a category of related records.,9,Findings,Perm,,VS,
Grouping Qualifier,VS,VSSCAT,Subcategory for Vital Signs,Char,SCAT,A further categorization of a measurement or examination.,10,Findings,Perm,,VS,
Record Qualifier,VS,VSPOS,Vital Signs Position of Subject,Char,POS,"Position of the subject during a measurement or examination. Examples: &quot;SUPINE&quot;, &quot;STANDING&quot;, &quot;SITTING&quot;.",11,Findings,Perm,(POSITION),VS,
Result Qualifier,VS,VSORRES,Result or Finding in Original Units,Char,ORRES,Result of the vital signs measurement as originally received or collected.,12,Findings,Exp,,VS,
Variable Qualifier,VS,VSORRESU,Original Units,Char,ORRESU,"Original units in which the data were collected. The unit for VSORRES. Examples: &quot;in&quot;, &quot;LB&quot;, &quot;beats/min&quot;.",13,Findings,Exp,(VSRESU),VS,
Result Qualifier,VS,VSSTRESC,Character Result/Finding in Std Format,Char,STRESC,"Contains the result value for all findings, copied or derived from VSORRES in a standard format or standard units. VSSTRESC should store all results or findings in character format; if results are numeric, they should also be stored in numeric format in VSSTRESN. For example, if a test has results &quot;NONE&quot;, &quot;NEG&quot;, and &quot;NEGATIVE&quot; in VSORRES, and these results effectively have the same meaning, they could be represented in standard format in VSSTRESC as &quot;NEGATIVE&quot;.",14,Findings,Exp,,VS,
Result Qualifier,VS,VSSTRESN,Numeric Result/Finding in Standard Units,Num,STRESN,Used for continuous or numeric results or findings in standard format; copied in numeric format from VSSTRESC. VSSTRESN should store all numeric test results or findings.,15,Findings,Exp,,VS,
Variable Qualifier,VS,VSSTRESU,Standard Units,Char,STRESU,Standardized unit used for VSSTRESC and VSSTRESN.,16,Findings,Exp,(VSRESU),VS,
Record Qualifier,VS,VSSTAT,Completion Status,Char,STAT,Used to indicate that a vital sign measurement was not done. Should be null if a result exists in VSORRES.,17,Findings,Perm,(ND),VS,
Record Qualifier,VS,VSREASND,Reason Not Performed,Char,REASND,Describes why a measurement or test was not performed. Examples: &quot;BROKEN EQUIPMENT&quot; or &quot;SUBJECT REFUSED&quot;. Used in conjunction with VSSTAT when value is &quot;NOT DONE&quot;.,18,Findings,Perm,,VS,
Record Qualifier,VS,VSLOC,Location of Vital Signs Measurement,Char,LOC,Location relevant to the collection of Vital Signs measurement. Example: &quot;ARM&quot; for blood pressure.,19,Findings,Perm,(LOC),VS,
Result Qualifier,VS,VSLAT,Laterality,Char,LAT,"Qualifier for anatomical location or specimen further detailing laterality. Examples: &quot;RIGHT&quot;, &quot;LEFT&quot;, &quot;BILATERAL&quot;.",20,Findings,Perm,(LAT),VS,
Record Qualifier,VS,VSLOBXFL,Last Observation Before Exposure Flag,Char,LOBXFL,Operationally-derived indicator used to identify the last non-missing value prior to RFXSTDTC. Should be &quot;Y&quot; or null.,21,Findings,Exp,(NY),VS,
Record Qualifier,VS,VSBLFL,Baseline Flag,Char,BLFL,Indicator used to identify a baseline value. Should be &quot;Y&quot; or null. Note that VSBLFL is retained for backward compatibility. The authoritative baseline for statistical analysis is in an ADaM dataset.,22,Findings,Perm,(NY),VS,
Record Qualifier,VS,VSDRVFL,Derived Flag,Char,DRVFL,"Used to indicate a derived record. The value should be &quot;Y&quot; or null. Records that represent the average of other records or that do not come from the CRF are examples of records that would be derived for the submission datasets. If VSDRVFL = &quot;Y,&quot; then VSORRES may be null, with VSSTRESC and (if numeric) VSSTRESN having the derived value.",23,Findings,Perm,(NY),VS,
Timing,VS,VISITNUM,Visit Number,Num,VISITNUM,"1. Clinical encounter number. \n 2. Numeric version of VISIT, used for sorting.",24,Findings,Exp,,,
Timing,VS,VISIT,Visit Name,Char,VISIT,Protocol-defined description of clinical encounter.May be used in addition to VISITNUM and/or VISITDY.,25,Findings,Perm,,,
Timing,VS,VISITDY,Planned Study Day of Visit,Num,VISITDY,Planned study day of the visit based upon RFSTDTC in Demographics.,26,Findings,Perm,,,
Timing,VS,TAETORD,Planned Order of Element within Arm,Num,TAETORD,Number that gives the planned order of the Element within the Arm.,27,Findings,Perm,,,
Timing,VS,EPOCH,Epoch,Char,EPOCH,Epoch associated with the start date/time at which the assessment was made.,28,Findings,Perm,(EPOCH),,
Timing,VS,VSDTC,Date/Time of Measurements,Char,DTC,Date and time of the vital signs assessment represented in ISO 8601 character format.,29,Findings,Exp,ISO 8601,VS,
Timing,VS,VSDY,Study Day of Vital Signs,Num,DY,"Study day of vital signs measurements, measured as integer days.Algorithm for calculations must be relative to the sponsor-defined RFSTDTC variable in Demographics.",30,Findings,Perm,,VS,
Timing,VS,VSTPT,Planned Time Point Name,Char,TPT,"Text description of time when measurement should be taken.This may be represented as an elapsed time relative to a fixed reference point, such as time of last dose. See VSTPTNUM and VSTPTREF. Examples: &quot;Start&quot;, &quot;5 min post&quot;.",31,Findings,Perm,,VS,
Timing,VS,VSTPTNUM,Planned Time Point Number,Num,TPTNUM,Numerical version of VSTPT to aid in sorting.,32,Findings,Perm,,VS,
Timing,VS,VSELTM,Planned Elapsed Time from Time Point Ref,Char,ELTM,"Planned elapsed time (in ISO 8601) relative to a planned fixed reference (VSTPTREF). This variable is useful where there are repetitive measures. Not a clock time or a date time variable. Represented as an ISO 8601 Duration. Examples: &quot;-PT15M&quot; to represent the period of 15 minutes prior to the reference point indicated by VSTPTREF, or &quot;PT8H&quot; to represent the period of 8 hours after the reference point indicated by VSTPTREF.",33,Findings,Perm,ISO 8601,VS,
Timing,VS,VSTPTREF,Time Point Reference,Char,TPTREF,"Name of the fixed reference point referred to by VSELTM, VSTPTNUM, and VSTPT. Examples: &quot;PREVIOUS DOSE&quot;, &quot;PREVIOUS MEAL&quot;.",34,Findings,Perm,,VS,
Timing,VS,VSRFTDTC,Date/Time of Reference Time Point,Char,RFTDTC,"Date/time of the reference time point, VSTPTREF.",35,Findings,Perm,ISO 8601,VS,
Identifier,FA,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Findings About,Req,,,
Identifier,FA,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Findings About,Req,FA,,
Identifier,FA,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product.,3,Findings About,Req,,,
Identifier,FA,FASEQ,Sequence Number,Num,SEQ,Sequence number given to ensure uniqueness of subject records within a domain. May be any valid number.,4,Findings About,Req,,FA,
Identifier,FA,FAGRPID,Group ID,Char,GRPID,Used to tie together a block of related records in a single domain for a subject.,5,Findings About,Perm,,FA,
Identifier,FA,FASPID,Sponsor-Defined Identifier,Char,SPID,Sponsor-defined reference number. Perhaps preprinted on the CRF as an explicit line identifier or defined in the sponsor's operational database. Example: Line number on a CRF.,6,Findings About,Perm,,FA,
Topic,FA,FATESTCD,Findings About Test Short Name,Char,TESTCD,"Short name of the measurement, test, or examination described in FATEST. It can be used as a column name when converting a dataset from a vertical to a horizontal format. The value in FATESTCD cannot be longer than 8 characters, nor can it start with a number (e.g., &quot;1TEST&quot; is not valid). FATESTCD cannot contain characters other than letters, numbers, or underscores. Examples: &quot;SEV&quot;, &quot;OCCUR&quot;. Note that controlled terminology is in several therapeutic area-specific codelists.",7,Findings About,Req,,FA,
Synonym Qualifier,FA,FATEST,Findings About Test Name,Char,TEST,"Verbatim name of the test or examination used to obtain the measurement or finding. The value in FATEST cannot be longer than 40 characters. Examples: &quot;Severity/Intensity&quot;, &quot;Occurrence&quot;. Note that controlled terminology is in several therapeutic area-specific codelists.",8,Findings About,Req,,FA,
Record Qualifier,FA,FAOBJ,Object of the Observation,Char,OBJ,"Used to describe the object or focal point of the findings observation that is represented by --TEST. Examples: the term (such as Acne) describing a clinical sign or symptom that is being measured by a Severity test, or an event such as VOMIT, where the volume of Vomit is being measured by a VOLUME test.",9,Findings About,Req,,FA,
Grouping Qualifier,FA,FACAT,Category for Findings About,Char,CAT,"Used to define a category of related records. Examples: &quot;GERD&quot;, &quot;PRE-SPECIFIED AE&quot;.",10,Findings About,Perm,,FA,
Grouping Qualifier,FA,FASCAT,Subcategory for Findings About,Char,SCAT,A further categorization of FACAT.,11,Findings About,Perm,,FA,
Result Qualifier,FA,FAORRES,Result or Finding in Original Units,Char,ORRES,Result of the test as originally received or collected.,12,Findings About,Exp,,FA,
Variable Qualifier,FA,FAORRESU,Original Units,Char,ORRESU,Original units in which the data were collected. The unit for FAORRES.,13,Findings About,Perm,(UNIT),FA,
Result Qualifier,FA,FASTRESC,Character Result/Finding in Std Format,Char,STRESC,"Contains the result value for all findings, copied or derived from FAORRES in a standard format or standard units. FASTRESC should store all results or findings in character format; if results are numeric, they should also be stored in numeric format in FASTRESN. For example, if a test has results &quot;NONE&quot;, &quot;NEG&quot;, and &quot;NEGATIVE&quot; in FAORRES, and these results effectively have the same meaning; they could be represented in standard format in FASTRESC as &quot;NEGATIVE&quot;.",14,Findings About,Exp,,FA,
Result Qualifier,FA,FASTRESN,Numeric Result/Finding in Standard Units,Num,STRESN,Used for continuous or numeric results or findings in standard format; copied in numeric format from FASTRESC. FASTRESN should store all numeric test results or findings.,15,Findings About,Perm,,FA,
Variable Qualifier,FA,FASTRESU,Standard Units,Char,STRESU,Standardized unit used for FASTRESC and FASTRESN.,16,Findings About,Perm,(UNIT),FA,
Record Qualifier,FA,FASTAT,Completion Status,Char,STAT,Used to indicate that the measurement was not done. Should be null if a result exists in FAORRES.,17,Findings About,Perm,(ND),FA,
Record Qualifier,FA,FAREASND,Reason Not Performed,Char,REASND,Describes why a question was not answered. Example: &quot;Subject refused&quot;. Used in conjunction with FASTAT when value is &quot;NOT DONE&quot;.,18,Findings About,Perm,,FA,
Record Qualifier,FA,FALOC,Location of the Finding About,Char,LOC,Used to specify the location of the clinical evaluation. Example: &quot;ARM&quot;.,19,Findings About,Perm,(LOC),FA,
Variable Qualifier,FA,FALAT,Laterality,Char,LAT,"Qualifier for anatomical location or specimen further detailing laterality. Examples: &quot;RIGHT&quot;, &quot;LEFT&quot;, &quot;BILATERAL&quot;.",20,Findings About,Perm,(LAT),FA,
Record Qualifier,FA,FALOBXFL,Last Observation Before Exposure Flag,Char,LOBXFL,Operationally-derived indicator used to identify the last non-missing value prior to RFXSTDTC. The value should be &quot;Y&quot; or null.,21,Findings About,Perm,(NY),FA,
Record Qualifier,FA,FABLFL,Baseline Flag,Char,BLFL,Indicator used to identify a baseline value. The value should be &quot;Y&quot; or null. Note that FABLFL is retained for backward compatibility. The authoritative baseline flag for statistical analysis is in an ADaM dataset.,22,Findings About,Perm,(NY),FA,
Record Qualifier,FA,FAEVAL,Evaluator,Char,EVAL,"Role of the person who provided the evaluation. Used only for results that are subjective (e.g., assigned by a person or a group). Should be null for records that contain collected or derived data. Examples: &quot;INVESTIGATOR&quot;, &quot;ADJUDICATION COMMITTEE&quot;, &quot;VENDOR&quot;.",23,Findings About,Perm,(EVAL),FA,
Timing,FA,VISITNUM,Visit Number,Num,VISITNUM,"1. Clinical encounter number. \n 2. Numeric version of VISIT, used for sorting.",24,Findings About,Exp,,,
Timing,FA,VISIT,Visit Name,Char,VISIT,Protocol-defined description of clinical encounter.May be used in addition to VISITNUM and/or VISITDY.,25,Findings About,Perm,,,
Timing,FA,VISITDY,Planned Study Day of Visit,Num,VISITDY,Planned study day of the visit based upon RFSTDTC in Demographics.,26,Findings About,Perm,,,
Timing,FA,TAETORD,Planned Order of Element within Arm,Num,TAETORD,Number that gives the planned order of the Element within the Arm.,27,Findings About,Perm,,,
Timing,FA,EPOCH,Epoch,Char,EPOCH,"Epoch associated with the date/time of the observation. Examples: &quot;SCREENING&quot;, &quot;TREATMENT&quot;, &quot;FOLLOW-UP&quot;.",28,Findings About,Perm,(EPOCH),,
Timing,FA,FADTC,Date/Time of Collection,Char,DTC,Collection date and time of findings assessment represented in ISO 8601 character format.,29,Findings About,Perm,ISO 8601,FA,
Timing,FA,FADY,Study Day of Collection,Num,DY,"Study day of collection, measured as integer days.Algorithm for calculations must be relative to the sponsor-defined RFSTDTC variable in Demographics. This formula should be consistent across the submission.",30,Findings About,Perm,,FA,
Identifier,SR,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Findings About,Req,,,
Identifier,SR,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Findings About,Req,SR,,
Identifier,SR,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across submission.,3,Findings About,Req,,,
Identifier,SR,SRSEQ,Sequence Number,Num,SEQ,Sequence number given to ensure uniqueness of subject records within a domain. May be any valid number.,4,Findings About,Req,,SR,
Identifier,SR,SRGRPID,Group ID,Char,GRPID,Used to tie together a block of related records in a single domain for a subject.,5,Findings About,Perm,,SR,
Identifier,SR,SRREFID,Reference ID,Char,REFID,Internal or external specimen identifier. Example: &quot;Specimen ID&quot;.,6,Findings About,Perm,,SR,
Identifier,SR,SRSPID,Sponsor-Defined Identifier,Char,SPID,Sponsor-defined identifier.,7,Findings About,Perm,,SR,
Topic,SR,SRTESTCD,Skin Response Test or Exam Short Name,Char,TESTCD,"Short name of the measurement, test, or examination described in SRTEST. It can be used as a column name when converting a dataset from a vertical to a horizontal format. The value in SRTESTCD cannot be longer than 8 characters, nor can it start with a number (e.g., &quot;1TEST&quot; is not valid). SRTESTCD cannot contain characters other than letters, numbers, or underscores.",8,Findings About,Req,(SRTESTCD),SR,
Synonym Qualifier,SR,SRTEST,Skin Response Test or Examination Name,Char,TEST,Verbatim name of the test or examination used to obtain the measurement or finding. The value in SRTEST cannot be longer than 40 characters. Example: &quot;Wheal Diameter&quot;.,9,Findings About,Req,(SRTEST),SR,
Record Qualifier,SR,SROBJ,Object of the Observation,Char,OBJ,"Used to describe the object or focal point of the findings observation that is represented by --TEST. Examples: the dose of the immunogenic material or the allergen associated with the response (e.g., &quot;Johnson Grass IgE 0.15 BAU mL&quot;).",10,Findings About,Req,,SR,
Grouping Qualifier,SR,SRCAT,Category for Test,Char,CAT,Used to define a category of Topic-variable values across subjects.,11,Findings About,Perm,,SR,
Grouping Qualifier,SR,SRSCAT,Subcategory for Test,Char,SCAT,A further categorization of SRCAT values.,12,Findings About,Perm,,SR,
Result Qualifier,SR,SRORRES,Results or Findings in Original Units,Char,ORRES,Results of measurement or finding as originally received or collected.,13,Findings About,Exp,,SR,
Variable Qualifier,SR,SRORRESU,Original Units,Char,ORRESU,Original units in which the data were collected. The unit for SRORRES. Example: &quot;mm&quot;.,14,Findings About,Exp,(UNIT),SR,
Result Qualifier,SR,SRSTRESC,Character Result/Finding in Std Format,Char,STRESC,"Contains the result value for all findings, copied or derived from SRORRES in a standard format or in standard units. SRSTRESC should store all results or findings in character format; if results are numeric, they should also be stored in numeric format in SRSTRESN.",15,Findings About,Exp,,SR,
Result Qualifier,SR,SRSTRESN,Numeric Results/Findings in Std. Units,Num,STRESN,Used for continuous or numeric results or findings in standard format; copied in numeric format from SRSTRESC. SRSTRESN should store all numeric test results or findings.,16,Findings About,Exp,,SR,
Variable Qualifier,SR,SRSTRESU,Standard Units,Char,STRESU,"Standardized units used for SRSTRESC and SRSTRESN, Example: &quot;mm&quot;.",17,Findings About,Exp,(UNIT),SR,
Record Qualifier,SR,SRSTAT,Completion Status,Char,STAT,Used to indicate exam not done. Should be null if a result exists in SRORRES.,18,Findings About,Perm,(ND),SR,
Record Qualifier,SR,SRREASND,Reason Not Done,Char,REASND,Describes why a measurement or test was not performed. Used in conjunction with SRSTAT when value is &quot;NOT DONE&quot;.,19,Findings About,Perm,,SR,
Record Qualifier,SR,SRNAM,Vendor Name,Char,NAM,Name or identifier of the laboratory or vendor who provided the test results.,20,Findings About,Perm,,SR,
Record Qualifier,SR,SRSPEC,Specimen Type,Char,SPEC,Defines the types of specimen used for a measurement. Example: &quot;SKIN&quot;.,21,Findings About,Perm,(SPECTYPE),SR,
Record Qualifier,SR,SRLOC,Location Used for Measurement,Char,LOC,Location relevant to the collection of the measurement.,22,Findings About,Perm,(LOC),SR,
Variable Qualifier,SR,SRLAT,Laterality,Char,LAT,"Qualifier for anatomical location further detailing laterality of intervention administration. Examples: &quot;RIGHT&quot;, &quot;LEFT&quot;, &quot;BILATERAL&quot;.",23,Findings About,Perm,(LAT),SR,
Record Qualifier,SR,SRMETHOD,Method of Test or Examination,Char,METHOD,"Method of test or examination. Examples: &quot;ELISA&quot;, &quot;EIA&quot;, &quot;MICRONEUTRALIZATION ASSAY&quot;, &quot;PRNT&quot; (Plaque Reduction Neutralization Tests).",24,Findings About,Perm,(METHOD),SR,
Record Qualifier,SR,SRLOBXFL,Last Observation Before Exposure Flag,Char,LOBXFL,Operationally-derived indicator used to identify the last non-missing value prior to RFXSTDTC. The value should be &quot;Y&quot; or null.,25,Findings About,Perm,(NY),SR,
Record Qualifier,SR,SRBLFL,Baseline Flag,Char,BLFL,Indicator used to identify a baseline value. The value should be &quot;Y&quot; or null. Note that SRBLFL is retained for backward compatibility. The authoritative baseline flag for statistical analysis is in an ADaM dataset.,26,Findings About,Perm,(NY),SR,
Record Qualifier,SR,SREVAL,Evaluator,Char,EVAL,"Role of person who provided evaluation. Used only for results that are subjective (e.g., assigned by a person or a group). Should be null for records that contain collected or derived data. Examples: &quot;INVESTIGATOR&quot;, &quot;ADJUDICATION COMMITTEE&quot;, &quot;VENDOR&quot;.",27,Findings About,Perm,(EVAL),SR,
Timing,SR,VISITNUM,Visit Number,Num,VISITNUM,"1. Clinical encounter number. \n 2. Numeric version of VISIT, used for sorting.",28,Findings About,Exp,,,
Timing,SR,VISIT,Visit Name,Char,VISIT,Protocol-defined description of clinical encounter.May be used in addition to VISITNUM and/or VISITDY.,29,Findings About,Perm,,,
Timing,SR,VISITDY,Planned Study Day of Visit,Num,VISITDY,Planned study day of the visit based upon RFSTDTC in Demographics.,30,Findings About,Perm,,,
Timing,SR,TAETORD,Planned Order of Element within Arm,Num,TAETORD,Number that gives the planned order of the Element within the Arm.,31,Findings About,Perm,,,
Timing,SR,EPOCH,Epoch,Char,EPOCH,"Epoch associated with the date/time of the observation. Examples: &quot;SCREENING&quot;, &quot;TREATMENT&quot;, and &quot;FOLLOW-UP&quot;.",32,Findings About,Perm,(EPOCH),,
Timing,SR,SRDTC,Date/Time of Collection,Char,DTC,Collection date and time of an observation represented in ISO 8601.,33,Findings About,Exp,ISO 8601,SR,
Timing,SR,SRDY,Study Day of Visit/Collection/Exam,Num,DY,Actual study day of visit/collection/exam expressed in integer days relative to sponsor- defined RFSTDTC in Demographics.,34,Findings About,Perm,,SR,
Timing,SR,SRTPT,Planned Time Point Name,Char,TPT,"Text description of time when measurement should be taken.This may be represented as an elapsed time relative to a fixed reference point, such as time of last dose. See SRTPTNUM and SRTPTREF. Examples: &quot;Start&quot;, &quot;5 min post&quot;.",35,Findings About,Perm,,SR,
Timing,SR,SRTPTNUM,Planned Time Point Number,Num,TPTNUM,Numerical version of SRTPT to aid in sorting.,36,Findings About,Perm,,SR,
Timing,SR,SRELTM,Planned Elapsed Time from Time Point Ref,Char,ELTM,"Planned elapsed time (in ISO 8601) relative to a fixed time point reference (SRTPTREF). Not a clock time or a date time variable. Represented as an ISO 8601 duration. Examples: &quot;-PT15M&quot; to represent the period of 15 minutes prior to the reference point indicated by EGTPTREF, or &quot;PT8H&quot; to represent the period of 8 hours after the reference point indicated by SRTPTREF.",37,Findings About,Perm,ISO 8601,SR,
Timing,SR,SRTPTREF,Time Point Reference,Char,TPTREF,"Name of the fixed reference point referred to by SRELTM, SRTPTNUM, and SRTPT. Example: &quot;INTRADERMAL INJECTION&quot;.",38,Findings About,Perm,,SR,
Timing,SR,SRRFTDTC,Date/Time of Reference Time Point,Char,RFTDTC,"Date/time of the reference time point, SRTPTREF.",39,Findings About,Perm,ISO 8601,SR,
Identifier,TA,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Trial Design,Req,,,
Identifier,TA,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Trial Design,Req,TA,,
Topic,TA,ARMCD,Planned Arm Code,Char,ARMCD,"ARMCD is limited to 20 characters and does not have special character restrictions. The maximum length of ARMCD is longer than that for other ""short"" variables to accommodate the kind of values that are likely to be needed for crossover trials. For example, if ARMCD values for a seven-period crossover were constructed using two-character abbreviations for each treatment and separating hyphens, the length of ARMCD values would be 20.",3,Trial Design,Req,,,
Synonym Qualifier,TA,ARM,Description of Planned Arm,Char,ARM,Name given to an Arm or treatment group.,4,Trial Design,Req,,,
Timing,TA,TAETORD,Planned Order of Element within Arm,Num,ETORD,Number that gives the order of the Element within the Arm.,5,Trial Design,Req,,TA,
Record Qualifier,TA,ETCD,Element Code,Char,ETCD,"ETCD (the companion to ELEMENT) is limited to 8 characters and does not have special character restrictions. These values should be short for ease of use in programming, but it is not expected that ETCD will need to serve as a variable name.",6,Trial Design,Req,,,
Synonym Qualifier,TA,ELEMENT,Description of Element,Char,ELEMENT,The name of the Element. The same Element may occur more than once within an Arm.,7,Trial Design,Perm,,,
Rule,TA,TABRANCH,Branch,Char,BRANCH,"Condition subject met, at a ""branch"" in the trial design at the end of this Element, to be included in this Arm (e.g., ""Randomization to DRUG X"").",8,Trial Design,Exp,,TA,
Rule,TA,TATRANS,Transition Rule,Char,TRANS,"If the trial design allows a subject to transition to an Element other than the next Element in sequence, then the conditions for transitioning to those other Elements, and the alternative Element sequences, are specified in this rule (e.g., ""Responders go to washout"").",9,Trial Design,Exp,,TA,
Timing,TA,EPOCH,Epoch,Char,EPOCH,Name of the Trial Epoch with which this Element of the Arm is associated.,10,Trial Design,Req,(EPOCH),,
Identifier,TD,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Trial Design,Req,,,
Identifier,TD,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Trial Design,Req,TD,,
Timing,TD,TDORDER,Sequence of Planned Assessment Schedule,Num,ORDER,A number given to ensure ordinal sequencing of the planned assessment schedules within a trial.,3,Trial Design,Req,,TD,
Timing,TD,TDANCVAR,Anchor Variable Name,Char,ANCVAR,"A reference to the date variable name that provides the start point from which the planned disease assessment schedule is measured. This must be a referenced from the ADaM ADSL dataset, e.g. ""ANCH1DT"". Note: TDANCVAR will contain the name of a reference date variable.",4,Trial Design,Req,,TD,
Timing,TD,TDSTOFF,Offset from the Anchor,Char,STOFF,A fixed offset from the date provided by the variable referenced in TDANCVAR. This is used when the timing of planned cycles does not start on the exact day referenced in the variable indicated in TDANCVAR. The value of this variable will be either zero or a positive value and will be represented in ISO 8601 character format.,5,Trial Design,Req,ISO 8601,TD,
Timing,TD,TDTGTPAI,Planned Assessment Interval,Char,TGTPAI,The planned interval between disease assessments represented in ISO 8601 character format.,6,Trial Design,Req,ISO 8601,TD,
Timing,TD,TDMINPAI,Planned Assessment Interval Minimum,Char,MINPAI,The lower limit of the allowed range for the planned interval between disease assessments represented in ISO 8601 character format.,7,Trial Design,Req,ISO 8601,TD,
Timing,TD,TDMAXPAI,Planned Assessment Interval Maximum,Char,MAXPAI,The upper limit of the allowed range for the planned interval between disease assessments represented in ISO 8601 character format.,8,Trial Design,Req,ISO 8601,TD,
Record Qualifier,TD,TDNUMRPT,Maximum Number of Actual Assessments,Num,NUMRPT,"This variable must represent the maximum number of actual assessments for the analysis that this disease assessment schedule describes. In a trial where the maximum number of assessments is not defined explicitly in the protocol (e.g., assessments occur until death), TDNUMRPT should represent the maximum number of disease assessments that support the efficacy analysis encountered by any subject across the trial at that point in time.",9,Trial Design,Req,,TD,
Identifier,TE,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Trial Design,Req,,,
Identifier,TE,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Trial Design,Req,TE,,
Topic,TE,ETCD,Element Code,Char,ETCD,"ETCD (the companion to ELEMENT) is limited to 8 characters and does not have special character restrictions. These values should be short for ease of use in programming, but it is not expected that ETCD will need to serve as a variable name.",3,Trial Design,Req,,,
Synonym Qualifier,TE,ELEMENT,Description of Element,Char,ELEMENT,The name of the Element.,4,Trial Design,Req,,,
Rule,TE,TESTRL,Rule for Start of Element,Char,STRL,Expresses rule for beginning Element.,5,Trial Design,Req,,TE,
Rule,TE,TEENRL,Rule for End of Element,Char,ENRL,Expresses rule for ending Element. Either TEENRL or TEDUR must be present for each Element.,6,Trial Design,Perm,,TE,
Timing,TE,TEDUR,Planned Duration of Element,Char,DUR,Planned Duration of Element in ISO 8601 format. Used when the rule for ending the Element is applied after a fixed duration.,7,Trial Design,Perm,ISO 8601,TE,
Identifier,TI,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Trial Design,Req,,,
Identifier,TI,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Trial Design,Req,TI,,
Topic,TI,IETESTCD,Incl/Excl Criterion Short Name,Char,IETESTCD,"Short name IETEST. It can be used as a column name when converting a dataset from a vertical to a horizontal format. The value in IETESTCD cannot be longer than 8 characters, nor can it start with a number (e.g., ""1TEST"" is not valid). IETESTCD cannot contain characters other than letters, numbers, or underscores. The prefix ""IE"" is used to ensure consistency with the IE domain.",3,Trial Design,Req,,,
Synonym Qualifier,TI,IETEST,Inclusion/Exclusion Criterion,Char,IETEST,Full text of the inclusion or exclusion criterion. The prefix "IE" is used to ensure consistency with the IE domain.,4,Trial Design,Req,,,
Grouping Qualifier,TI,IECAT,Inclusion/Exclusion Category,Char,IECAT,Used for categorization of the inclusion or exclusion criteria.,5,Trial Design,Req,(IECAT),,
Grouping Qualifier,TI,IESCAT,Inclusion/Exclusion Subcategory,Char,IESCAT,"A further categorization of the exception criterion. Can be used to distinguish criteria for a sub-study or to categorize as major or minor exceptions. Examples: ""MAJOR"", ""MINOR"".",6,Trial Design,Perm,,,
Rule,TI,TIRL,Inclusion/Exclusion Criterion Rule,Char,RL,Rule that expresses the criterion in computer-executable form. See Assumption 4.,7,Trial Design,Perm,,TI,
Record Qualifier,TI,TIVERS,Protocol Criteria Versions,Char,VERS,The number of this version of the Inclusion/Exclusion criteria. May be omitted if there is only one version.,8,Trial Design,Perm,,TI,
Identifier,TM,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Trial Design,Req,,,
Identifier,TM,DOMAIN,Domain,Char,DOMAIN,"Two-character abbreviation for the domain, which must be TM.",2,Trial Design,Req,TM,,
Topic,TM,MIDSTYPE,Disease Milestone Type,Char,MIDSTYPE,The type of Disease Milestone. Example: "HYPOGLYCEMIC EVENT".,3,Trial Design,Req,,,
Rule,TM,TMDEF,Disease Milestone Definition,Char,DEF,Definition of the Disease Milestone.,4,Trial Design,Req,,TM,
Record Qualifier,TM,TMRPT,Disease Milestone Repetition Indicator,Char,RPT,Indicates whether this is a Disease Milestone that can occur only once ("N") or a type of Disease Milestone that can occur multiple times ("Y").,5,Trial Design,Req,(NY),TM,
Identifier,TS,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Trial Design,Req,,,
Identifier,TS,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Trial Design,Req,TS,,
Identifier,TS,TSSEQ,Sequence Number,Num,SEQ,Sequence number given to ensure uniqueness within a dataset. Allows inclusion of multiple records for the same TSPARMCD.,3,Trial Design,Req,,TS,
Identifier,TS,TSGRPID,Group ID,Char,GRPID,Used to tie together a group of related records.,4,Trial Design,Perm,,TS,
Topic,TS,TSPARMCD,Trial Summary Parameter Short Name,Char,PARMCD,"TSPARMCD (the companion to TSPARM) is limited to 8 characters and does not have special character restrictions. These values should be short for ease of use in programming, but it is not expected that TSPARMCD will need to serve as variable names. Examples: ""AGEMIN"", ""AGEMAX"".",5,Trial Design,Req,(TSPARMCD),TS,
Synonym Qualifier,TS,TSPARM,Trial Summary Parameter,Char,PARM,"Term for the Trial Summary Parameter. The value in TSPARM cannot be longer than 40 characters. Examples: ""Planned Minimum Age of Subjects"", ""Planned Maximum Age of Subjects"".",6,Trial Design,Req,(TSPARM),TS,
Result Qualifier,TS,TSVAL,Parameter Value,Char,VAL,Value of TSPARM. Example: "ASTHMA" when TSPARM value is "Trial Indication". TSVAL can only be null when TSVALNF is populated. Text over 200 characters can be added to additional columns TSVAL1-TSVALn. See Assumption 8.,7,Trial Design,Exp,,TS,
Result Qualifier,TS,TSVALNF,Parameter Null Flavor,Char,VALNF,"Null flavor for the value of TSPARM, to be populated if and only if TSVAL is null.",8,Trial Design,Perm,ISO 21090 NullFlavor enumeration,TS,
Result Qualifier,TS,TSVALCD,Parameter Value Code,Char,VALCD,"This is the code of the term in TSVAL. For example, ""6CW7F3G59X"" is the code for Gabapentin; ""C49488"" is the code for Y. The length of this variable can be longer than 8 to accommodate the length of the external terminology.",9,Trial Design,Exp,,TS,
Result Qualifier,TS,TSVCDREF,Name of the Reference Terminology,Char,VCDREF,"The name of the Reference Terminology from which TSVALCD is taken. For example; CDISC, SNOMED, ISO 8601.",10,Trial Design,Exp,,TS,
Result Qualifier,TS,TSVCDVER,Version of the Reference Terminology,Char,VCDVER,"The version number of the Reference Terminology, if applicable.",11,Trial Design,Exp,,TS,
Identifier,TV,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Trial Design,Req,,,
Identifier,TV,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Trial Design,Req,TV,,
Topic,TV,VISITNUM,Visit Number,Num,VISITNUM,"1. Clinical encounter number \n 2. Numeric version of VISIT, used for sorting.",3,Trial Design,Req,,,
Synonym Qualifier,TV,VISIT,Visit Name,Char,VISIT,Protocol-defined description of clinical encounter.May be used in addition to VISITNUM and/or VISITDY as a text description of the clinical encounter.,4,Trial Design,Perm,,,
Timing,TV,VISITDY,Planned Study Day of Visit,Num,VISITDY,"Planned study day of VISIT.Due to its sequential nature, used for sorting.",5,Trial Design,Perm,,,
Record Qualifier,TV,ARMCD,Planned Arm Code,Char,ARMCD,"ARMCD is limited to 20 characters and does not have special character restrictions. The maximum length of ARMCD is longer than for other &quot;short&quot; variables to accommodate the kind of values that are likely to be needed for crossover trials. For example, if ARMCD values for a seven-period crossover were constructed using two-character abbreviations for each treatment and separating hyphens, the length of ARMCD values would be 20.If the timing of Visits for a trial does not depend on which Arm a subject is in, then ARMCD should be null.",6,Trial Design,Exp,,,
Synonym Qualifier,TV,ARM,Description of Planned Arm,Char,ARM,"Name given to an Arm or Treatment Group.If the timing of Visits for a trial does not depend on which Arm a subject is in, then Arm should be left blank.",7,Trial Design,Perm,,,
Rule,TV,TVSTRL,Visit Start Rule,Char,STRL,"Rule describing when the Visit starts, in relation to the sequence of Elements.",8,Trial Design,Req,,TV,
Rule,TV,TVENRL,Visit End Rule,Char,ENRL,"Rule describing when the Visit ends, in relation to the sequence of Elements.",9,Trial Design,Perm,,TV,
Identifier,RELREC,STUDYID,,Char,STUDYID,Unique identifier for a study.,1,Relationship,Req,,,Study Identifier
Identifier,RELREC,RDOMAIN,,Char,RDOMAIN,Abbreviation for the domain of the parent record(s).,2,Relationship,Req,(DOMAIN),,Related Domain Abbreviation
Identifier,RELREC,USUBJID,,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product.,3,Relationship,Exp,,,Unique Subject Identifier
Identifier,RELREC,IDVAR,,Char,IDVAR,Name of the identifying variable in the general-observation-class dataset that identifies the related record(s). Examples include --SEQ and --GRPID.,4,Relationship,Req,,,Identifying Variable
Identifier,RELREC,IDVARVAL,,Char,IDVARVAL,"Value of identifying variable described in IDVAR. If --SEQ is the variable being used to describe this record, then the value of --SEQ would be entered here.",5,Relationship,Exp,,,Identifying Variable Value
Record Qualifier,RELREC,RELTYPE,,Char,RELTYPE,"Identifies the hierarchical level of the records in the relationship. Values should be either ONE or MANY. Used only when identifying a relationship between datasets (as described in Section 8.3, Relating Datasets).",6,Relationship,Exp,(RELTYPE),,Relationship Type
Record Qualifier,RELREC,RELID,,Char,RELID,"Unique value within USUBJID that identifies the relationship. All records for the same USUBJID that have the same RELID are considered ""related/associated."" RELID can be any value the sponsor chooses, and is only meaningful within the RELREC dataset to identify the related/associated Domain records.",7,Relationship,Req,,,Relationship Identifier
Identifier,RELSUB,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Relationship,Req,,,
Identifier,RELSUB,USUBJID,Unique Subject Identifier,Char,USUBJID,Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product. Either USUBJID or POOLID must be populated.,2,Relationship,Exp,,,
Identifier,RELSUB,POOLID,Pool Identifier,Char,POOLID,"Identifier used to identify a pool of subjects. If POOLID is entered, POOLDEF records must exist for each subject in the pool and USUBJID must be null. Either USUBJID or POOLID must be populated.",3,Relationship,Perm,,,
Identifier,RELSUB,RSUBJID,Related Subject or Pool Identifier,Char,RSUBJID,Identifier used to identify a related subject or pool of subjects. RSUBJID will be populated with either the USUBJID of the related subject or the POOLID of the related pool.,4,Relationship,Req,,,
Record Qualifier,RELSUB,SREL,Subject Relationship,Char,SREL,Describes the relationship of the subject identified in USUBJID or the pool identified in POOLID to the subject or pool identified in RSUBJID.,5,Relationship,Req,(RELSUB),,
Identifier,SUPPQUAL,STUDYID,Study Identifier,Char,STUDYID,Study identifier of the parent record(s).,1,Relationship,Req,,,
Identifier,SUPPQUAL,RDOMAIN,Related Domain Abbreviation,Char,RDOMAIN,Two-character abbreviation for the domain of the parent record(s).,2,Relationship,Req,(DOMAIN),,
Identifier,SUPPQUAL,USUBJID,Unique Subject Identifier,Char,USUBJID,Unique subject identifier of the parent record(s).,3,Relationship,Req,,,
Identifier,SUPPQUAL,IDVAR,Identifying Variable,Char,IDVAR,"Identifying variable in the dataset that identifies the related record(s). Examples: --SEQ, --GRPID.",4,Relationship,Exp,,,
Identifier,SUPPQUAL,IDVARVAL,Identifying Variable Value,Char,IDVARVAL,Value of identifying variable of the parent record(s).,5,Relationship,Exp,,,
Topic,SUPPQUAL,QNAM,Qualifier Variable Name,Char,QNAM,"The short name of the Qualifier variable, which is used as a column name in a domain view with data from the parent domain. The value in QNAM cannot be longer than 8 characters, nor can it start with a number (e.g., ""1TEST"" is not valid). QNAM cannot contain characters other than letters, numbers, or underscores. This will often be the column name in the sponsor's operational dataset.",6,Relationship,Req,,,
Synonym Qualifier,SUPPQUAL,QLABEL,Qualifier Variable Label,Char,QLABEL,This is the long name or label associated with QNAM. The value in QLABEL cannot be longer than 40 characters. This will often be the column label in the sponsor's original dataset.,7,Relationship,Req,,,
Result Qualifier,SUPPQUAL,QVAL,Data Value,Char,QVAL,"Result of, response to, or value associated with QNAM. A value for this column is required; no records can be in SUPP-- with a null value for QVAL.",8,Relationship,Req,,,
Record Qualifier,SUPPQUAL,QORIG,Origin,Char,QORIG,"Since QVAL can represent a mixture of collected (on a CRF), derived, or assigned items, QORIG is used to indicate the origin of this data. Examples include ""CRF"", ""Assigned"", or ""Derived"". See Section 4.1.8, Origin Metadata.",9,Relationship,Req,,,
Record Qualifier,SUPPQUAL,QEVAL,Evaluator,Char,QEVAL,"Used only for results that are subjective (e.g., assigned by a person or a group). Should be null for records that contain objectively collected or derived data. Some examples include ""ADJUDICATION COMMITTEE"", ""STATISTICIAN"", ""DATABASE ADMINISTRATOR"", ""CLINICAL COORDINATOR"", etc.",10,Relationship,Exp,,,
Identifier,OI,STUDYID,Study Identifier,Char,STUDYID,Unique identifier for a study.,1,Study Reference,Req,,,
Identifier,OI,DOMAIN,Domain Abbreviation,Char,DOMAIN,Two-character abbreviation for the domain.,2,Study Reference,Req,OI,,
Identifier,OI,NHOID,Non-host Organism Identifier,Char,NHOID,Sponsor-defined identifier for a non-host organism. NHOID should be populated with an intuitive name based on the identity of the organism as reported by the lab. It must be unique for each unique organism as defined by the specific values of the organism's entire known taxonomy described by pairs of OIPARMCD and OIVAL .,3,Study Reference,Req,,,
Identifier,OI,OISEQ,Sequence Number,Num,SEQ,Sequence number to given to ensure uniqueness within a parameter within an organism (NHOID) within dataset.,4,Study Reference,Req,,OI,
Topic,OI,OIPARMCD,Non-host Organism ID Element Short Name,Char,PARMCD,"Short name of the taxon being described. Examples: ""GROUP"", ""GENTYP"", ""SUBTYP"".",5,Study Reference,Req,,OI,
Synonym Qualifier,OI,OIPARM,Non-host Organism ID Element Name,Char,PARM,"Name of the taxon being described. Examples: ""Group"", ""Genotype"", ""Subtype"".",6,Study Reference,Req,,OI,
Result Qualifier,OI,OIVAL,Non-host Organism ID Element Value,Char,VAL,Value for the taxon in OIPARMCD/OIPARM for the organism identified by NHOID.,7,Study Reference,Req,,OI,