The following timing variables are available for use in any domain based on one of the 3 general observation classes, except where restricted in the assumptions for the standard domain models in the implementation guides. See Section 3.2, Special-purpose Domains, for additional guidance relating to special-purpose domains.

All Observation Classes—Timing Variables

SDTM v2.1 Metadata Check for Class and Dataset Specification Table Beta 1

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#Variable NameVariable LabelTypeFormatRoleVariable(s) QualifiedUsage RestrictionsVariable C-codeDefinitionNotesExamples
1VISITNUMVisit NumberNum
Timing

C83101

An assigned numeric identifier that aligns to the chronological order of a clinical encounter.

Numeric version of VISIT, used for sorting. VISITNUM does not have to be an integer value.

1, 1.1, 503.75
2VISITVisit NameChar
Timing

C171010The label for a protocol-defined clinical encounter.

3VISITDYPlanned Study Day of VisitNum
Timing

C171011The planned study day of a clinical encounter relative to the sponsor-defined reference start date.Should be an integer.
4TAETORDPlanned Order of Element Within ArmNum
Timing

C83438An assigned numeric identifier that gives the planned order of the element within the trial arm of the study.See Section 5.1.1.2, Trial Arms.
5EPOCHEpochChar
Timing

C71738A time period defined in the protocol with a study-specific purpose.The epoch associated with an observation is determined by the start date or start date and time of the observation, or the date/time of collection if start date/time is not collected (see Section 5.1.1.2, Trial Arms).
6RPHASERepro PhaseChar
Timing
Not in human clinical trials

Reproductive phase with which the reproductive stage of the reproductive path is associated. Defined in Trial Paths domain. The RPHASE variable is Required when any Reproductive Phase Day variable is used.


7RPPLDYPlanned Repro Phase Day of ObservationNum
Timing
Not in human clinical trialsC170506The day within the reproductive phase on which the test or observation was scheduled to occur.Expressed as an integer.
8RPPLSTDYPlanned Repro Phase Day of Obs StartNum
Timing
Not in human clinical trialsC170508The day within the reproductive phase on which the test or observation was scheduled to begin.Expressed as an integer.
9RPPLENDYPlanned Repro Phase Day of Obs EndNum
Timing
Not in human clinical trialsC170507The day within the reproductive phase on which the test or observation was scheduled to end.Expressed as an integer.
10--DTCDate/Time of CollectionChar

ISO 8601 datetime or interval

Timing

C82515The date or date and time of the assessment or the specimen or data collection from the subject, represented in a standardized character format.

11--STDTCStart Date/Time of ObservationCharISO 8601 datetime or intervalTiming

Not in Findings class domains

C82517The start date or date and time of an intervention or event, represented in a standardized character format.The start date of a Findings class record is stored in the --DTC variable.
12--ENDTCEnd Date/Time of ObservationCharISO 8601 datetime or intervalTiming

C82516The end date or date and time of an intervention, event, or finding, represented in a standardized character format.

13--DYStudy Day of Visit/Collection/ExamNum
Timing


C170993The number of days from the sponsor-defined reference start date to the date of collection (--DTC), used in study data tabulation.The sponsor-defined reference start date is RFSTDTC in Demographics.
14--STDYStudy Day of Start of ObservationNum
Timing
Not in Findings class domainsC171005The number of days from the sponsor-defined reference start date to the start of an intervention or event (--STDTC), used for study data tabulation.The sponsor-defined reference start date is RFSTDTC in Demographics.
15--ENDYStudy Day of End of ObservationNum
Timing

C170995The number of days from the sponsor-defined reference start date to the end of an intervention, event, or finding (--ENDTC), used for study data tabulation.The sponsor-defined reference start date is RFSTDTC in Demographics.
16--NOMDYNominal Study Day for TabulationsNum
Timing
Not in human clinical trialsC170498The nominal study day, relative to the sponsor-defined reference start date, used by data collection and reporting systems for grouping records for observations that may be scheduled to occur on different days into a single study day (e.g., for output on a tabulation report).

17--NOMLBLLabel for Nominal Study DayChar
Timing
Not in human clinical trialsC170499The name for a protocol-defined nominal study day.As presented in the study report.
18--RPDYActual Repro Phase Day of ObservationNum
Timing
Not in human clinical trialsC170504The day within the reproductive phase on which the test or observation occurred.Expressed as an integer.
19--RPSTDYActual Repro Phase Day of Obs StartNum
Timing
Not in human clinical trialsC170509The day within the reproductive phase on which the test or observation began.Expressed as an integer.
20--RPENDYActual Repro Phase Day of Obs EndNum
Timing
Not in human clinical trialsC170505The day within the reproductive phase on which the test or observation ended.Expressed as an integer.
21--XDYDay of Obs Relative to Exposure

Num


Timing




The actual study day of an intervention, event, or finding, derived relative to the first exposure to any protocol-specified treatment or product. Expressed in integer days relative to RFXSTDTC in Demographics.


22--XSTDYStart Day of Obs Relative to ExposureNum
Timing
Not in Findings class domains

The actual study day of the start of an intervention or event, derived relative to the first exposure to any protocol-specified treatment or product. Expressed in integer days relative to RFXSTDTC in Demographics.


23--XENDYEnd Day of Obs Relative to Exposure

Num


Timing



The actual study day of the end of an intervention, event, or finding, derived relative to the first exposure to any protocol-specified treatment or product. Expressed in integer days relative to RFXSTDTC in Demographics.


24--CHDYDay of Obs Rel to Challenge Agent

Num


Timing



The actual study day of an intervention, event, or finding, derived relative to the first exposure to the challenge agent that induces the disease or condition that the investigational treatment is intended to cure, mitigate, treat, or prevent. Expressed in integer days relative to RFCSTDTC in Demographics.


25--CHSTDYStart Day of Obs Rel to Challenge Agent

Num


Timing
Not in Findings class domains

The actual study day of the start of an intervention or event derived relative to the first exposure to the challenge agent that induces the disease or condition that the investigational treatment is intended to c ure, mitigate, treat, or prevent. Expressed in integer days relative to RFCSTDTC in Demographics.


26--CHENDYEnd Day of Obs Rel to Challenge Agent

Num


Timing



The actual study day of the end of an intervention, event, or finding derived relative to the first exposure to the challenge agent that induces the disease or condition that the investigational treatment is intended to cure, mitigate, treat, or prevent. Expressed in integer days relative to RFCSTDTC in Demographics.


27--DURCollected DurationCharISO 8601 durationTiming

C170992The collected length of time during which an observation continues, represented in a standardized character format.Used only if collected on the CRF and not derived.
28--TPTPlanned Time Point NameChar
Timing

C171029

The description of the time when a protocol-defined activity is planned to occur, used for study data tabulation.

This may be represented as an elapsed time relative to a fixed reference point (e.g., time since last dose). See --TPTNUM and --TPTREF."PREDOSE", "1 HOUR POST-DOSE"
29--TPTNUMPlanned Time Point NumberNum
Timing

C82545The numeric identifier of when an observation is planned to occur.Used in sorting.
30--ELTMPlanned Elapsed Time from Time Point RefCharISO 8601 durationTiming

C170994The interval of time between a planned time point and a fixed reference point, represented in a standardized character format.The fixed reference point is in --TPTREF. This variable is useful where there are repetitive measures. Not a clock time or a date/time variable, but an interval.
31--TPTREFTime Point ReferenceChar
Timing

C171030The description of a time point that acts as a fixed reference for a series of planned time points, used for study data tabulation.

Description of the fixed reference point referred to by --ELTM, --TPTNUM, --TPT, --STINT, and --ENINT.

"PREVIOUS DOSE", "PREVIOUS MEAL"
32--RFTDTCDate/Time of Reference Time PointCharISO 8601 datetime or intervalTiming

C82518The actual date or date and time of a time point that acts as a fixed reference for a series of planned time points, represented in a standardized character format.The fixed reference point is in --TPTREF.
33--STRFStart Relative to Reference PeriodChar
Timing

C82559The characterization of the start of an observation relative to the study 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.
34--ENRFEnd Relative to Reference PeriodChar
Timing

C82557The characterization of the end of an observation relative to the study 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.
35--EVLINTEvaluation IntervalChar

ISO 8601 duration or interval

Timing

C82534The planned time interval for which an observation is assessed, represented in a standardized character format.Usually used with --DTC to describe an interval of this duration that ended at the time represented in --DTC."-P2M" to represent a period of the past 2 months as the evaluation interval for a question from a questionnaire.
36--EVINTXEvaluation Interval TextChar
Timing

C117044A textual description of the planned time interval for which an observation is assessed, where the interval is not able to be represented in a standardized character format.A value that cannot be represented in ISO 8601 format."LIFETIME", "LAST NIGHT", "RECENTLY", "OVER THE LAST FEW WEEKS"
37--STRTPTStart Relative to Reference Time PointChar
Timing

C82560The characterization of the start of an observation relative to a reference time point.The sponsor-defined reference time point is in --STTPT.
38--STTPTStart Reference Time PointChar
Timing

C82575The description or date and/or time of a time point that acts as a fixed reference for characterizing the start of an observation.This is the sponsor-defined reference point referred to by --STRTPT."2003-12-15", "VISIT 1"
39--ENRTPTEnd Relative to Reference Time PointChar
Timing

C82558The characterization of the end of an observation relative to a reference time point.The sponsor-defined reference time point is in --ENTPT.
40--ENTPTEnd Reference Time PointChar
Timing

C82574The description or date and/or time of a time point that acts as a fixed reference for characterizing the end of an observation.This is the sponsor-defined reference point referred to by --ENRTPT."2003-12-25", "VISIT 2"
41MIDSDisease Milestone Instance NameChar
Timing



The name of a specific instance of a Disease Milestone Type (MIDSTYPE) described in the Trial Disease Milestones dataset (see Section 5.1.4.3, Trial Disease Milestones). This should be unique within a subject. Used only in conjunction with RELMIDS and MIDSDTC.
42RELMIDSTemporal Relation to Milestone InstanceChar
Timing



The temporal relationship of the observation to the Disease Milestone Instance Name in MIDS."IMMEDIATELY BEFORE", "AT TIME OF", "AFTER"
43MIDSDTCDisease Milestone Instance Date/TimeCharISO 8601 datetime or intervalTiming



The start date/time of the Disease Milestone Instance Name in MIDS.
44--STINTPlanned Start of Assessment IntervalCharISO 8601 durationTiming


C117061The start of a planned assessment interval relative to a reference time point, represented in a standardized character format.The reference time point is in --TPTREF. As this variable describes planned timing of an assessment, caution should be exercised when using outside of the Findings class of domains. In an Events or Interventions domain, it may refer to the interval over which --OCCUR is assessed.
45--ENINTPlanned End of Assessment IntervalCharISO 8601 durationTiming

C117042The end of a planned assessment interval relative to a reference time point, represented in a standardized character format.The reference time point is in --TPTREF. As this variable describes planned timing of an assessment, caution should be exercised when using outside of the Findings class of domains. In an Events or Interventions domain, it may refer to the interval over which --OCCUR is assessed.
46--DETECTTime in Days to DetectionNum
Timing


Not in human clinical trials

C117041The number of days from the start of dosing to the earliest detection of a condition or pathogen.

47--PTFLPoint in Time FlagChar
Timing

Only in Findings class specimen-based domains: BS, CP, GF, IS, LB, MB, MS, MI, PC, PP



An indication that the specimen was collected at a single point in time. The value is "Y" or null.


48--PDURPlanned DurationCharISO 8601 durationTiming
Only in Findings class specimen-based domains: BS, CP, GF, IS, LB, MB, MS, MI, PC, PP


Planned duration of a finding. For a sample-based finding, this could apply to the planned duration of specimen collection.


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