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Variable NameVariable LabelTypeCodelist/Controlled TermsCoreNotes
STUDYIDStudy IdentifierChar
ReqDM.STUDYID
USUBJIDUnique Subject IdentifierChar
ReqDM.USUBJID
SUBJIDSubject Identifier for the StudyChar
ReqDM.SUBJID
SITEIDStudy Site IdentifierChar
ReqDM.SITEID
AGEAgeNum
ReqDM.AGE. If analysis needs require a derived age that does not match DM.AGE, then AAGE must be added
AGEUAge UnitsChar(AGEU)ReqDM.AGEU
AGEGRyPooled Age Group yChar
PermCharacter description of a grouping or pooling of the subject's age for analysis purposes. For example, AGEGR1 might have values of "<18", "18-65", and ">65"; AGEGR2 might have values of "Less than 35 y old" and "At least 35 y old".
SEXSexCharSEX)ReqDM.SEX
RACERaceChar(RACE)ReqDM.RACE
RACEGRyPooled Race Group yChar
PermCharacter description of a grouping or pooling of the subject's race for analysis purposes.
ETHNICEthnicityChar
PermDM.ETHNIC
SAFFLSafety Population FlagCharY; NCondY if ADSL.TR01SDT is not null, otherwise N
PPROTFLPer-Protocol Population FlagCharY; NCondY if ADSL.SAFFL=Y and at least one post-baseline assessment was done, otherwise N
RANDFLRandomized Population FlagCharY; NCondY if the subject was randomized, otherwise N
ARMDescription of Planned ArmChar
ReqDM.ARM
ACTARMDescription of Actual ArmChar
PermDM.ACTARM
TRTxxPPlanned Treatment for Period xxChar
ReqSubject-level identifier that represents the planned treatment for period xx. In a one-period randomized trial, TRT01P would be the treatment to which the subject was randomized. TRTxxP might be derived from the SDTM DM variable ARM. At least TRT01P is required.
TRTxxPNPlanned Treatment for Period xx (N)Num
PermNumeric representation of TRTxxP. There must be a one-to-one relationship between TRTxxPN and TRTxxP within a study.
TRTxxPN cannot be present unless TRTxxP is also present. When TRTxxP and TRTxxPN are present, then on a given record, either both must be populated or both must be null.
TRTxxAActual Treatment for Period xxChar
CondSubject-level identifier that represents the actual treatment for the subject for period xx. Required when actual treatment does not match planned and there is an analysis of the data as treated.
TRTxxANActual Treatment for Period xx (N)Num
Perm

Numeric representation of TRTxxA. There must be a one-to-one relationship between TRTxxAN and TRTxxA within a study.

TRTxxAN cannot be present unless TRTxxA is also present. When TRTxxA and TRTxxAN are present, then on a given record, either both must be populated or both must be null.

TRTSEQP
Char
CondRequired when there is an analysis based on the sequence of treatments, for example in a crossover design. TRTSEQP is not necessarily equal to ARM, for example if ARM contains elements that are not relevant to analysis of treatments or ARM is not fully descriptive (e.g., "GROUP 1," "GROUP 2"). When analyzing based on the sequence of treatments, TRTSEQP is required even if identical to ARM.
TRTSDTDate of First Exposure to TreatmentNum
CondDate of first exposure to treatment for a subject in a study. TRTSDT and/or TRTSDTM are required if there is an investigational product. Note that TRTSDT is not required to have the same value as the SDTM DM variable RFXSTDTC. While both of these dates reflect the concept of first exposure, the ADaM date may be derived to support the analysis which may not necessarily be the very first date in the SDTM EX domain.
TRTSDTMDatetime of First Exposure to TreatmentNum
CondDatetime of first exposure to treatment for a subject in a study. TRTSDT and/or TRTSDTM are required if there is an investigational product.
TRTEDTDate of Last Exposure to TreatmentNum
CondDate of last exposure to treatment for a subject in a study. TRTEDT and/or TRTEDTM are required if there is an investigational product. Note that TRTEDT is not required to have the same value as the SDTM DM variable RFXENDTC. While both of these dates reflect the concept of last exposure, the ADaM date may be derived to support the analysis which may not necessarily be the very last date in the SDTM EX domain.
TRTEDTMDatetime of Last Exposure to TreatmentNum
CondDatetime of last exposure to treatment for a subject in a study. TRTEDT and/or TRTEDTM are required if there is an investigational product.
TRxxSDTDate of First Exposure in Period xxNum
CondDate of first exposure to treatment in period xx. TRxxSDT and/or TRxxSDTM are only required in trial designs where multiple treatment periods are defined (i.e., required when there is a TRTxxP other than TRT01P). Examples include crossover designs or designs where multiple periods exist for the same treatment.
TRxxEDTDate of Last Exposure in Period xxNum
CondDate of last exposure to treatment in period xx. TRxxEDT and/or TRxxEDTM are only required in trial designs where multiple treatment periods are defined (i.e., required when there is a TRTxxP other than TRT01P).
APHASEwDescription of Phase wChar
PermDescription of analysis phase w. Analysis phase is independent of TRTxxP within ADSL, and may be populated for spans of time where a subject is not on treatment.
EOSSTTEnd of Study StatusChar(SBJTSTAT)PermThe subject's status as of the end of study or data cutoff. Examples: COMPLETED, DISCONTINUED, ONGOING.
EOSDTEnd of Study DateNum
PermDate subject ended the study - either date of completion or date of discontinuation or data cutoff date for interim analyses.
DCSREASReason for Discontinuation from StudyChar
PermReason for subject's discontinuation from study. The source would most likely be the SDTM DS dataset. Null for subjects who completed the study.
DCSREASPDCSREASP
Reason Spec for Discont from Study
Char
PermAdditional detail regarding subject's discontinuation from study (e.g., description of "other").
EOTSTTEnd of Treatment StatusChar(SBJTSTAT)PermThe subject's status as of the end of treatment or data cutoff. Examples: COMPLETED, DISCONTINUED, ONGOING.
DCTREASReason for Discontinuation of TreatmentChar
PermIf a subject discontinued treatment in the study, then this variable indicates the reason for discontinuation. This is for discontinuation of treatment in the overall study and not to be used for discontinuation reason within individual treatment periods.
DCTREASPReason Specify for Discont of TreatmentChar
PermAdditional detail regarding subject's discontinuation from treatment (e.g., description of "other").
RFICDTDate of Informed ConsentNum
PermDate subject gave informed consent. Generally equivalent to DM.RFICDTC.
ENRLDTDate of EnrollmentNum
PermDate of subject's enrollment into trial.
RANDDTDate of RandomizationNum
CondRequired in randomized trials.
LSTALVDTDate Last Known AliveNum
PermIf this variable is included in ADSL, the best practice is to populate it for everyone. If the derivation for subjects who died differs from the derivation for subjects who are not known to have died, the differences should be noted in metadata.
TRTDURDTotal Treatment Duration (Days)Num
PermTotal treatment duration, as measured in days. More than one of TRTDURD, TRTDURM, and TRTDURY can be populated, but each represents the entire duration in its respective units.
DTHDTDate of DeathNum
PermDate of subject's death. Derived from DM.DTHDTC.
DTHCAUSCause of DeathChar
PermCause of Death.
STRATARStrata Used for RandomizationChar
PermSTRATAR contains the combination of values of the individual stratification factors used for randomization. The exact format should be determined by the sponsor. This variable is intended for studies that use stratified randomization. For example, ">=50, Treatment experienced, N"
STRATAVStrata from Verification SourceChar
PermSTRATAV contains the entire string value represents the combination of values of the individual stratification factors that should have been used and represents the "as verified" value. The STRATAV variables are based on the source documentation and are determined after randomization. If the values used for the randomization of a given subject were all correct, then STRATAV will equal STRATAR. Otherwise, one or more components of the text string for STRATAR and STRATAV will be different.
The exact format should be determined by the sponsor. For example, ">=50, Treatment experienced, Y"

Variable NameVariable LabelTypeCodelist/Controlled TermsCoreNotes
STUDYIDStudy IdentifiertextABC123ReqDM.STUDYID
USUBJIDUnique Subject Identifiertext
ReqDM.USUBJID
SUBJIDSubject Identifier for the Studytext
ReqDM.SUBJID
SITEIDStudy Site Identifiertext01;02ReqDM.SITEID
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STUDYIDUSUBJIDSUBJIDSITEIDAGEAGEUAGEGR1SEXRACEETHNICSAFFLRANDFLARMACTARMTRT01PTRT01PNTRT01ATRT01ANTRTSDTTRTEDTEOSSTTEOSDTDCSREAS
ABC123ABC12301001010010157YEARS<65MWHITENOT HISPANIC OR LATINOYYProduct AProduct AProduct A1Product A12006-01-122006-03-10COMPLETED2003-09-29
ABC123ABC12301002010020150YEARS
MWHITENOT HISPANIC OR LATINOYYBProduct BProduct B2Product B22006-01-152006-02-28DISCONTINUED
LOST TO FOLLOW-UP
ABC123ABC123ABC12301003010030168YEARS
FBLACK OR AFRICAN AMERICANNOT HISPANIC OR LATINOYYBProduct BProduct B2Product B22006-01-162006-03-19COMPLETED

ABC123ABC123010040100401


MASIANNOT HISPANIC OR LATINONN







DISCONTINUED
SCREEN FAILURE
ABC123ABC12302001020010255YEARS
FAMERICAN INDIAN OR ALASKA NATIVENOT HISPANIC OR LATINOYYBProduct BProduct B2Product B22006-02-022006-03-31COMPLETED

ABC123ABC12302002020020249YEARS
FNATIVE HAWAIIAN OR OTHER PACIFIC ISLANDERSNOT HISPANIC OR LATINOYYAProduct AProduct A1Product A12006-02-032006-04-05DISCONTINUED
ADVERSE EVENT
ABC123ABC123020030200302


FMULTIPLENOT HISPANIC OR LATINONN







DISCONTINUED
SCREEN FAILURE

Dataset Debug Message

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