Observation Class: Findings - Domain: Inclusion/Exclusion Criteria Not Met

  1. StudyEvent: ODM
    1. Observation Class: Special Purpose - Domain: Comments
    2. Observation Class: Special Purpose - Domain: Demographics
    3. Observation Class: Special Purpose - Domain: Subject Elements
    4. Observation Class: Special Purpose - Domain: Subject Disease Milestones
    5. Observation Class: Special Purpose - Domain: Subject Visits
    6. Observation Class: Interventions - Domain: Procedure Agents
    7. Observation Class: Interventions - Domain: Concomitant/Prior Medications
    8. Observation Class: Interventions - Domain: Exposure
    9. Observation Class: Interventions - Domain: Exposure as Collected
    10. Observation Class: Interventions - Domain: Meal Data
    11. Observation Class: Interventions - Domain: Procedures
    12. Observation Class: Interventions - Domain: Substance Use
    13. Observation Class: Events - Domain: Adverse Events
    14. Observation Class: Events - Domain: Clinical Events
    15. Observation Class: Events - Domain: Disposition
    16. Observation Class: Events - Domain: Protocol Deviations
    17. Observation Class: Events - Domain: Healthcare Encounters
    18. Observation Class: Events - Domain: Medical History
    19. Observation Class: Findings - Domain: Drug Accountability
    20. Observation Class: Findings - Domain: Death Details
    21. Observation Class: Findings - Domain: ECG Test Results
    22. Observation Class: Findings - Domain: Inclusion/Exclusion Criteria Not Met
    23. Observation Class: Findings - Domain: Immunogenicity Specimen Assessments
    24. Observation Class: Findings - Domain: Laboratory Test Results
    25. Observation Class: Findings - Domain: Microbiology Specimen
    26. Observation Class: Findings - Domain: Microbiology Susceptibility
    27. Observation Class: Findings - Domain: Microscopic Findings
    28. Observation Class: Findings - Domain: Morphology
    29. Observation Class: Findings - Domain: Cardiovascular System Findings
    30. Observation Class: Findings - Domain: Musculoskeletal System Findings
    31. Observation Class: Findings - Domain: Nervous System Findings
    32. Observation Class: Findings - Domain: Ophthalmic Examinations
    33. Observation Class: Findings - Domain: Reproductive System Findings
    34. Observation Class: Findings - Domain: Respiratory System Findings
    35. Observation Class: Findings - Domain: Urinary System Findings
    36. Observation Class: Findings - Domain: Pharmacokinetics Concentrations
    37. Observation Class: Findings - Domain: Pharmacokinetics Parameters
    38. Observation Class: Findings - Domain: Physical Examination
    39. Observation Class: Findings - Domain: Functional Tests
    40. Observation Class: Findings - Domain: Questionnaires
    41. Observation Class: Findings - Domain: Disease Response and Clin Classification
    42. Observation Class: Findings - Domain: Subject Characteristics
    43. Observation Class: Findings - Domain: Subject Status
    44. Observation Class: Findings - Domain: Tumor/Lesion Identification
    45. Observation Class: Findings - Domain: Tumor/Lesion Results
    46. Observation Class: Findings - Domain: Vital Signs
    47. Observation Class: Findings - Domain: Findings About Events or Interventions
    48. Observation Class: Findings - Domain: Skin Response
    49. Observation Class: Trial Design - Domain: Trial Arms
    50. Observation Class: Trial Design - Domain: Trial Elements
    51. Observation Class: Trial Design - Domain: Trial Visits
    52. Observation Class: Trial Design - Domain: Trial Disease Assessments
    53. Observation Class: Trial Design - Domain: Trial Disease Milestones
    54. Observation Class: Trial Design - Domain: Trial Inclusion/Exclusion Criteria
    55. Observation Class: Trial Design - Domain: Trial Summary Information
    56. Observation Class: Relationships - Domain: Related Records
    57. Observation Class: Relationships - Domain: Supplemental Qualifiers for [domain name]
    58. Observation Class: Relationships - Domain: Related Subjects
    59. Observation Class: Study Reference - Domain: Non-host Organism Identifiers
Inclusion/Exclusion Criteria Not Met
Description

Inclusion/Exclusion Criteria Not Met

Alias
SDTMIG v3.3
IE
UMLS CUI-1
C1512693
UMLS CUI-2
C0680251
UMLS CUI-3
C0231175
NCIt V19.10d:
C61536
Study Identifier
Description

Role: Identifier CDISC Notes (for domains) Description (for General Classes): Unique identifier for a study. Controlled Terms or Format (if applicable): NA

Data type

text

Alias
UMLS CUI [1]
C2826693
SDTMIG 3.3
STUDYID
NCIt V19.10d
C83082
Domain Abbreviation
Description

Role: Identifier CDISC Notes (for domains) Description (for General Classes): Two-character abbreviation for the domain. Controlled Terms or Format (if applicable): IE

Data type

text

Alias
UMLS CUI [1,1]
C1883204
UMLS CUI [1,2]
C0000723
SDTMIG 3.3
DOMAIN
NCIt V19.10d
NCIt V19.10d
Unique Subject Identifier
Description

Role: Identifier CDISC Notes (for domains) Description (for General Classes): Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product. Controlled Terms or Format (if applicable): NA

Data type

text

Alias
UMLS CUI [1,1]
C1710548
UMLS CUI [1,2]
C2826693
SDTMIG 3.3
USUBJID
NCIt V19.10d
C70731
Sequence Number
Description

Role: Identifier CDISC Notes (for domains) Description (for General Classes): Sequence number given to ensure uniqueness of subject records within a domain. May be any valid number. Controlled Terms or Format (if applicable): NA

Data type

integer

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C2348184
UMLS CUI [2,1]
C0680251
UMLS CUI [2,2]
C2348184
SDTMIG 3.3
IESEQ
NCIt V19.10d
C83299
Sponsor-Defined Identifier
Description

Role: Identifier CDISC Notes (for domains) Description (for General Classes): 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. Controlled Terms or Format (if applicable): NA

Data type

text

Alias
UMLS CUI [1,1]
C2347796
UMLS CUI [1,2]
C0600091
SDTMIG 3.3
IESPID
NCIt V19.10d
C83300
Inclusion/Exclusion Criterion Short Name
Description

Role: Topic CDISC Notes (for domains) Description (for General Classes): 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., "1TEST" is not valid). IETESTCD cannot contain characters other than letters, numbers, or underscores. Examples: "IN01", "EX01". Controlled Terms or Format (if applicable): NA

Data type

text

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C1806781
UMLS CUI [1,3]
C0027365
UMLS CUI [2,1]
C0680251
UMLS CUI [2,2]
C1806781
UMLS CUI [2,3]
C0027365
SDTMIG 3.3
IETESTCD
NCIt V19.10d
C83144
Inclusion/Exclusion Criterion
Description

Role: Synonym Qualifier CDISC Notes (for domains) Description (for General Classes): 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. Controlled Terms or Format (if applicable): NA

Data type

text

Alias
UMLS CUI [1]
C1512693
UMLS CUI [2]
C0680251
SDTMIG 3.3
IETEST
NCIt V19.10d
C83147
Inclusion/Exclusion Category
Description

Role: Grouping Qualifier CDISC Notes (for domains) Description (for General Classes): Used to define a category of related records across subjects. Controlled Terms or Format (if applicable): (IECAT), not extensible

Data type

text

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0683312
UMLS CUI [2,1]
C0680251
UMLS CUI [2,2]
C0683312
SDTMIG 3.3
IECAT
NCIt V19.10d
C83016
Inclusion/Exclusion Subcategory
Description

Role: Grouping Qualifier CDISC Notes (for domains) Description (for General Classes): 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: "MAJOR", "MINOR". Controlled Terms or Format (if applicable): NA

Data type

text

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C1515010
UMLS CUI [2,1]
C0680251
UMLS CUI [2,2]
C1515010
SDTMIG 3.3
IESCAT
NCIt V19.10d
C83298
I/E Criterion Original Result
Description

Role: Result Qualifier CDISC Notes (for domains) Description (for General Classes): Original response to Inclusion/Exclusion Criterion question, i.e., whether the inclusion or exclusion criterion was met. Controlled Terms or Format (if applicable): (NY), not extensbile

Data type

text

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0205313
UMLS CUI [1,3]
C1274040
UMLS CUI [2,1]
C0680251
UMLS CUI [2,2]
C0205313
UMLS CUI [2,3]
C1274040
SDTMIG 3.3
IEORRES
NCIt V19.10d
C83297
I/E Criterion Result in Std Format
Description

Role: Result Qualifier CDISC Notes (for domains) Description (for General Classes): Response to Inclusion/Exclusion criterion result in standard format. Controlled Terms or Format (if applicable): (NY), not extensible

Data type

text

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C1274040
UMLS CUI [1,3]
C1442989
UMLS CUI [1,4]
C1301627
UMLS CUI [2,1]
C0680251
UMLS CUI [2,2]
C1274040
UMLS CUI [2,3]
C1442989
UMLS CUI [2,4]
C1301627
SDTMIG 3.3
IESTRESC
NCIt V19.10d
C83301
Visit Number
Description

Role: Timing CDISC Notes (for domains) Description (for General Classes): 1. Clinical encounter number. 2. Numeric version of VISIT, used for sorting. Controlled Terms or Format (if applicable): NA

Data type

integer

Alias
UMLS CUI [1]
C1549755
SDTMIG 3.3
VISITNUM
NCIt V19.10d
C83101
Visit Name
Description

Role: Timing CDISC Notes (for domains) Description (for General Classes): 1. Protocol-defined description of clinical encounter. 2. May be used in addition to VISITNUM and/or VISITDY. Controlled Terms or Format (if applicable): NA

Data type

text

Alias
UMLS CUI [1]
C2826704
SDTMIG 3.3
VISIT
NCIt V19.10d
C83093
Planned Study Day of Visit
Description

Role: Timing CDISC Notes (for domains) Description (for General Classes): Planned study day of the visit based upon RFSTDTC in Demographics. Controlled Terms or Format (if applicable): NA

Data type

text

Alias
UMLS CUI [1,1]
C1301732
UMLS CUI [1,2]
C2826182
UMLS CUI [1,3]
C0545082
SDTMIG 3.3
VISITDY
NCIt V19.10d
C83450
Planned Order of Element within Arm
Description

Role: Timing CDISC Notes (for domains) Description (for General Classes): Number that gives the planned order of the Element within the Arm for the Element in which the assessment was made. Controlled Terms or Format (if applicable): NA

Data type

integer

Alias
UMLS CUI [1,1]
C1301732
UMLS CUI [1,2]
C1705175
UMLS CUI [1,3]
C3812827
UMLS CUI [1,4]
C1522541
SDTMIG 3.3
TAETORD
NCIt V19.10d
C83438
Epoch
Description

Role: Timing CDISC Notes (for domains) Description (for General Classes): Epoch associated with the observation date/time of the inclusion/exclusion finding. Controlled Terms or Format (if applicable): (EPOCH), extensible

Data type

text

Alias
UMLS CUI [1]
C2347803
SDTMIG 3.3
EPOCH
NCIt V19.10d
C71738
Date/Time of Collection
Description

Role: Timing CDISC Notes (for domains) Description (for General Classes): Collection date and time of the inclusion/exclusion criterion represented in ISO 8601 character format. Controlled Terms or Format (if applicable): ISO 8601

Data type

datetime

Alias
UMLS CUI [1,1]
C1264639
UMLS CUI [1,2]
C1512693
UMLS CUI [1,3]
C1516698
UMLS CUI [2,1]
C1264639
UMLS CUI [2,2]
C0680251
UMLS CUI [2,3]
C1516698
SDTMIG 3.3
IEDTC
NCIt V19.10d
C83295
Study Day of Collection
Description

Role: Timing CDISC Notes (for domains) Description (for General Classes): 1. Study day of collection of the inclusion/exclusion exceptions, measured as integer days. 2. Algorithm for calculations must be relative to the sponsor-defined RFSTDTC variable in Demographics. This formula should be consistent across the submission. Controlled Terms or Format (if applicable): NA

Data type

integer

Measurement units
  • d
Alias
UMLS CUI [1,1]
C2826182
UMLS CUI [1,2]
C1512693
UMLS CUI [1,3]
C1516698
UMLS CUI [2,1]
C2826182
UMLS CUI [2,2]
C0680251
UMLS CUI [2,3]
C1516698
SDTMIG 3.3
IEDY
NCIt V19.10d
C83296
d

Similar models

Observation Class: Findings - Domain: Inclusion/Exclusion Criteria Not Met

  1. StudyEvent: ODM
    1. Observation Class: Special Purpose - Domain: Comments
    2. Observation Class: Special Purpose - Domain: Demographics
    3. Observation Class: Special Purpose - Domain: Subject Elements
    4. Observation Class: Special Purpose - Domain: Subject Disease Milestones
    5. Observation Class: Special Purpose - Domain: Subject Visits
    6. Observation Class: Interventions - Domain: Procedure Agents
    7. Observation Class: Interventions - Domain: Concomitant/Prior Medications
    8. Observation Class: Interventions - Domain: Exposure
    9. Observation Class: Interventions - Domain: Exposure as Collected
    10. Observation Class: Interventions - Domain: Meal Data
    11. Observation Class: Interventions - Domain: Procedures
    12. Observation Class: Interventions - Domain: Substance Use
    13. Observation Class: Events - Domain: Adverse Events
    14. Observation Class: Events - Domain: Clinical Events
    15. Observation Class: Events - Domain: Disposition
    16. Observation Class: Events - Domain: Protocol Deviations
    17. Observation Class: Events - Domain: Healthcare Encounters
    18. Observation Class: Events - Domain: Medical History
    19. Observation Class: Findings - Domain: Drug Accountability
    20. Observation Class: Findings - Domain: Death Details
    21. Observation Class: Findings - Domain: ECG Test Results
    22. Observation Class: Findings - Domain: Inclusion/Exclusion Criteria Not Met
    23. Observation Class: Findings - Domain: Immunogenicity Specimen Assessments
    24. Observation Class: Findings - Domain: Laboratory Test Results
    25. Observation Class: Findings - Domain: Microbiology Specimen
    26. Observation Class: Findings - Domain: Microbiology Susceptibility
    27. Observation Class: Findings - Domain: Microscopic Findings
    28. Observation Class: Findings - Domain: Morphology
    29. Observation Class: Findings - Domain: Cardiovascular System Findings
    30. Observation Class: Findings - Domain: Musculoskeletal System Findings
    31. Observation Class: Findings - Domain: Nervous System Findings
    32. Observation Class: Findings - Domain: Ophthalmic Examinations
    33. Observation Class: Findings - Domain: Reproductive System Findings
    34. Observation Class: Findings - Domain: Respiratory System Findings
    35. Observation Class: Findings - Domain: Urinary System Findings
    36. Observation Class: Findings - Domain: Pharmacokinetics Concentrations
    37. Observation Class: Findings - Domain: Pharmacokinetics Parameters
    38. Observation Class: Findings - Domain: Physical Examination
    39. Observation Class: Findings - Domain: Functional Tests
    40. Observation Class: Findings - Domain: Questionnaires
    41. Observation Class: Findings - Domain: Disease Response and Clin Classification
    42. Observation Class: Findings - Domain: Subject Characteristics
    43. Observation Class: Findings - Domain: Subject Status
    44. Observation Class: Findings - Domain: Tumor/Lesion Identification
    45. Observation Class: Findings - Domain: Tumor/Lesion Results
    46. Observation Class: Findings - Domain: Vital Signs
    47. Observation Class: Findings - Domain: Findings About Events or Interventions
    48. Observation Class: Findings - Domain: Skin Response
    49. Observation Class: Trial Design - Domain: Trial Arms
    50. Observation Class: Trial Design - Domain: Trial Elements
    51. Observation Class: Trial Design - Domain: Trial Visits
    52. Observation Class: Trial Design - Domain: Trial Disease Assessments
    53. Observation Class: Trial Design - Domain: Trial Disease Milestones
    54. Observation Class: Trial Design - Domain: Trial Inclusion/Exclusion Criteria
    55. Observation Class: Trial Design - Domain: Trial Summary Information
    56. Observation Class: Relationships - Domain: Related Records
    57. Observation Class: Relationships - Domain: Supplemental Qualifiers for [domain name]
    58. Observation Class: Relationships - Domain: Related Subjects
    59. Observation Class: Study Reference - Domain: Non-host Organism Identifiers
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Inclusion/Exclusion Criteria Not Met
IE (SDTMIG v3.3)
C1512693 (UMLS CUI-1)
C0680251 (UMLS CUI-2)
C0231175 (UMLS CUI-3)
C61536 (NCIt V19.10d:)
STUDYID
Item
Study Identifier
text
C2826693 (UMLS CUI [1])
STUDYID (SDTMIG 3.3)
C83082 (NCIt V19.10d)
DOMAIN
Item
Domain Abbreviation
text
C1883204 (UMLS CUI [1,1])
C0000723 (UMLS CUI [1,2])
DOMAIN (SDTMIG 3.3)
NCIt V19.10d (NCIt V19.10d)
USUBJID
Item
Unique Subject Identifier
text
C1710548 (UMLS CUI [1,1])
C2826693 (UMLS CUI [1,2])
USUBJID (SDTMIG 3.3)
C70731 (NCIt V19.10d)
SEQ
Item
Sequence Number
integer
C1512693 (UMLS CUI [1,1])
C2348184 (UMLS CUI [1,2])
C0680251 (UMLS CUI [2,1])
C2348184 (UMLS CUI [2,2])
IESEQ (SDTMIG 3.3)
C83299 (NCIt V19.10d)
SPID
Item
Sponsor-Defined Identifier
text
C2347796 (UMLS CUI [1,1])
C0600091 (UMLS CUI [1,2])
IESPID (SDTMIG 3.3)
C83300 (NCIt V19.10d)
TESTCD
Item
Inclusion/Exclusion Criterion Short Name
text
C1512693 (UMLS CUI [1,1])
C1806781 (UMLS CUI [1,2])
C0027365 (UMLS CUI [1,3])
C0680251 (UMLS CUI [2,1])
C1806781 (UMLS CUI [2,2])
C0027365 (UMLS CUI [2,3])
IETESTCD (SDTMIG 3.3)
C83144 (NCIt V19.10d)
TEST
Item
Inclusion/Exclusion Criterion
text
C1512693 (UMLS CUI [1])
C0680251 (UMLS CUI [2])
IETEST (SDTMIG 3.3)
C83147 (NCIt V19.10d)
Item
Inclusion/Exclusion Category
text
C1512693 (UMLS CUI [1,1])
C0683312 (UMLS CUI [1,2])
C0680251 (UMLS CUI [2,1])
C0683312 (UMLS CUI [2,2])
IECAT (SDTMIG 3.3)
C83016 (NCIt V19.10d)
Code List
Inclusion/Exclusion Category
CL Item
EXCLUSION (EXCLUSION)
C0680251 (UMLS CUI-1)
C25370 (NCIt V19.10d)
CL Item
INCLUSION (INCLUSION)
C1512693 (UMLS CUI-1)
C25532 (NCIt V19.10d)
SCAT
Item
Inclusion/Exclusion Subcategory
text
C1512693 (UMLS CUI [1,1])
C1515010 (UMLS CUI [1,2])
C0680251 (UMLS CUI [2,1])
C1515010 (UMLS CUI [2,2])
IESCAT (SDTMIG 3.3)
C83298 (NCIt V19.10d)
Item
I/E Criterion Original Result
text
C1512693 (UMLS CUI [1,1])
C0205313 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C0680251 (UMLS CUI [2,1])
C0205313 (UMLS CUI [2,2])
C1274040 (UMLS CUI [2,3])
IEORRES (SDTMIG 3.3)
C83297 (NCIt V19.10d)
Code List
I/E Criterion Original Result
CL Item
No (N)
C1298908 (UMLS CUI-1)
C49487 (NCIt V19.10d)
CL Item
NA; Not Applicable (NA)
C1272460 (UMLS CUI-1)
C48660 (NCIt V19.10d)
CL Item
U; UNK; Unknown (U)
C0439673 (UMLS CUI-1)
C17998 (NCIt V19.10d)
CL Item
Yes (Y)
C1705108 (UMLS CUI-1)
C49488 (NCIt V19.10d)
Item
I/E Criterion Result in Std Format
text
C1512693 (UMLS CUI [1,1])
C1274040 (UMLS CUI [1,2])
C1442989 (UMLS CUI [1,3])
C1301627 (UMLS CUI [1,4])
C0680251 (UMLS CUI [2,1])
C1274040 (UMLS CUI [2,2])
C1442989 (UMLS CUI [2,3])
C1301627 (UMLS CUI [2,4])
IESTRESC (SDTMIG 3.3)
C83301 (NCIt V19.10d)
Code List
I/E Criterion Result in Std Format
CL Item
No (N)
C1298908 (UMLS CUI-1)
C49487 (NCIt V19.10d)
CL Item
NA; Not Applicable (NA)
C1272460 (UMLS CUI-1)
C48660 (NCIt V19.10d)
CL Item
U; UNK; Unknown (U)
C0439673 (UMLS CUI-1)
C17998 (NCIt V19.10d)
CL Item
Yes (Y)
C1705108 (UMLS CUI-1)
C49488 (NCIt V19.10d)
VISITNUM
Item
Visit Number
integer
C1549755 (UMLS CUI [1])
VISITNUM (SDTMIG 3.3)
C83101 (NCIt V19.10d)
VISIT
Item
Visit Name
text
C2826704 (UMLS CUI [1])
VISIT (SDTMIG 3.3)
C83093 (NCIt V19.10d)
VISITDY
Item
Planned Study Day of Visit
text
C1301732 (UMLS CUI [1,1])
C2826182 (UMLS CUI [1,2])
C0545082 (UMLS CUI [1,3])
VISITDY (SDTMIG 3.3)
C83450 (NCIt V19.10d)
TAETORD
Item
Planned Order of Element within Arm
integer
C1301732 (UMLS CUI [1,1])
C1705175 (UMLS CUI [1,2])
C3812827 (UMLS CUI [1,3])
C1522541 (UMLS CUI [1,4])
TAETORD (SDTMIG 3.3)
C83438 (NCIt V19.10d)
Item
Epoch
text
C2347803 (UMLS CUI [1])
EPOCH (SDTMIG 3.3)
C71738 (NCIt V19.10d)
Code List
Epoch
CL Item
BASELINE (BASELINE)
C1552824 (UMLS CUI-1)
C125938 (NCIt V19.10d)
CL Item
BLINDED TREATMENT (BLINDED TREATMENT)
C3640651 (UMLS CUI-1)
C102255 (NCIt V19.10d)
CL Item
Continuation Phase (CONTINUATION TREATMENT)
C4055184 (UMLS CUI-1)
C123452 (NCIt V19.10d)
CL Item
FOLLOW-UP (FOLLOW-UP)
C3274571 (UMLS CUI-1)
C99158 (NCIt V19.10d)
CL Item
Induction Phase; Intensive Phase (INDUCTION TREATMENT)
C4049995 (UMLS CUI-1)
C123453 (NCIt V19.10d)
CL Item
LONG-TERM FOLLOW-UP (LONG-TERM FOLLOW-UP)
C1517942 (UMLS CUI-1)
C16032 (NCIt V19.10d)
CL Item
OPEN LABEL TREATMENT (OPEN LABEL TREATMENT)
C3640652 (UMLS CUI-1)
C102256 (NCIt V19.10d)
CL Item
RUN-IN (RUN-IN)
C3274438 (UMLS CUI-1)
C98779 (NCIt V19.10d)
CL Item
SCREENING (SCREENING)
C1710477 (UMLS CUI-1)
C48262 (NCIt V19.10d)
CL Item
TREATMENT (TREATMENT)
C3538994 (UMLS CUI-1)
C101526 (NCIt V19.10d)
CL Item
WASHOUT (WASHOUT)
C1710661 (UMLS CUI-1)
C42872 (NCIt V19.10d)
DTC
Item
Date/Time of Collection
datetime
C1264639 (UMLS CUI [1,1])
C1512693 (UMLS CUI [1,2])
C1516698 (UMLS CUI [1,3])
C1264639 (UMLS CUI [2,1])
C0680251 (UMLS CUI [2,2])
C1516698 (UMLS CUI [2,3])
IEDTC (SDTMIG 3.3)
C83295 (NCIt V19.10d)
DY
Item
Study Day of Collection
integer
C2826182 (UMLS CUI [1,1])
C1512693 (UMLS CUI [1,2])
C1516698 (UMLS CUI [1,3])
C2826182 (UMLS CUI [2,1])
C0680251 (UMLS CUI [2,2])
C1516698 (UMLS CUI [2,3])
IEDY (SDTMIG 3.3)
C83296 (NCIt V19.10d)