English

Observation Class: Events - Domain: Disposition

59 forms  
  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
Disposition
Description

Disposition

Alias
SDTMIG v3.3
DS
NCIt V19.10d:
C49576
UMLS CUI-1
C0743223
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): DS

Data type

text

Alias
UMLS CUI [1,1]
C1883204
UMLS CUI [1,2]
C0000723
SDTMIG 3.3
DOMAIN
NCIt V19.10d
C49556
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]
C0743223
UMLS CUI [1,2]
C2348184
SDTMIG 3.3
DSSEQ
NCIt V19.10d
C83249
Group ID
Description

Role: Identifier CDISC Notes (for domains) Description (for General Classes): Used to tie together a block of related records in a single domain for a subject. Controlled Terms or Format (if applicable): NA

Data type

text

Alias
UMLS CUI [1,1]
C0743223
UMLS CUI [1,2]
C0441833
UMLS CUI [1,3]
C0600091
SDTMIG 3.3
DSGRPID
NCIt V19.10d
C83247
Reference ID
Description

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

Data type

text

Alias
UMLS CUI [1,1]
C0743223
UMLS CUI [1,2]
C2826265
SDTMIG 3.3
DSREFID
NCIt V19.10d
C87866
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: Line number on a Disposition page. Controlled Terms or Format (if applicable): NA

Data type

text

Alias
UMLS CUI [1,1]
C0743223
UMLS CUI [1,2]
C2347796
UMLS CUI [1,3]
C0600091
SDTMIG 3.3
DSSPID
NCIt V19.10d
C83250
Reported Term for the Disposition Event
Description

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

Data type

text

Alias
UMLS CUI [1,1]
C2826302
UMLS CUI [1,2]
C0743223
SDTMIG 3.3
DSTERM
NCIt V19.10d
C74590
Standardized Disposition Term
Description

Role: Synonym Qualifier CDISC Notes (for domains) Description (for General Classes): 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. Controlled Terms or Format (if applicable): (NCOMPLT), (PROTMLST), both extensible; NCOMPLT added as codelist, entries from PROTMLST added as well and marked as being part of PROTMLST in the respective comment section.

Data type

text

Alias
UMLS CUI [1,1]
C0743223
UMLS CUI [1,2]
C1442989
UMLS CUI [1,3]
C0027365
SDTMIG 3.3
DSDECOD
NCIt V19.10d
C89968
Category for Disposition Event
Description

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

Data type

text

Alias
UMLS CUI [1,1]
C0683312
UMLS CUI [1,2]
C0743223
SDTMIG 3.3
DSCAT
NCIt V19.10d
C83245
Subcategory for Disposition Event
Description

Role: Grouping Qualifier CDISC Notes (for domains) Description (for General Classes): A further categorization of DSCAT (e.g., "STUDY PARTICIPATION", "STUDY TREATMENT" when DSCAT = "DISPOSITION EVENT"). Controlled Terms or Format (if applicable): NA

Data type

text

Alias
UMLS CUI [1,1]
C0743223
UMLS CUI [1,2]
C0441471
UMLS CUI [1,3]
C1515010
SDTMIG 3.3
DSSCAT
NCIt V19.10d
C83248
Epoch
Description

Role: Timing CDISC Notes (for domains) Description (for General Classes): Epoch associated with the start date/time of the event. 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 disposition observation 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]
C0743223
UMLS CUI [1,3]
C1516698
SDTMIG 3.3
DSDTC
NCIt V19.10d
C83246
Start Date/Time of Disposition Event
Description

Role: Timing CDISC Notes (for domains) Description (for General Classes): Start date/time of the disposition event in ISO 8601 character format. Controlled Terms or Format (if applicable): ISO 8601

Data type

datetime

Alias
UMLS CUI [1,1]
C0808070
UMLS CUI [1,2]
C0743223
UMLS CUI [2,1]
C1301880
UMLS CUI [2,2]
C0743223
SDTMIG 3.3
DSSTDTC
NCIt V19.10d
C83251
Study Day of Collection
Description

Role: Timing CDISC Notes (for domains) Description (for General Classes): Start date/time of the disposition event in ISO 8601 character format. Controlled Terms or Format (if applicable): NA

Data type

datetime

Alias
UMLS CUI [1,1]
C0743223
UMLS CUI [1,2]
C2826182
UMLS CUI [1,3]
C1516698
SDTMIG 3.3
DSDY
NCIt V19.10d
C82437
NCIt V19.10d-2
C49576
Study Day of Start of Disposition Event
Description

Role: Timing CDISC Notes (for domains) Description (for General Classes): Study day of start of event relative to the sponsor-defined RFSTDTC. Controlled Terms or Format (if applicable): NA

Data type

text

Alias
UMLS CUI [1,1]
C2826182
UMLS CUI [1,2]
C0439659
UMLS CUI [1,3]
C0743223
SDTMIG 3.3
DSSTDY
NCIt V19.10d
C83252
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Similar models

Observation Class: Events - Domain: Disposition

59 forms
  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
Disposition
DS (SDTMIG v3.3)
C49576 (NCIt V19.10d:)
C0743223 (UMLS CUI-1)
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)
C49556 (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
C0743223 (UMLS CUI [1,1])
C2348184 (UMLS CUI [1,2])
DSSEQ (SDTMIG 3.3)
C83249 (NCIt V19.10d)
GRPID
Item
Group ID
text
C0743223 (UMLS CUI [1,1])
C0441833 (UMLS CUI [1,2])
C0600091 (UMLS CUI [1,3])
DSGRPID (SDTMIG 3.3)
C83247 (NCIt V19.10d)
REFID
Item
Reference ID
text
C0743223 (UMLS CUI [1,1])
C2826265 (UMLS CUI [1,2])
DSREFID (SDTMIG 3.3)
C87866 (NCIt V19.10d)
SPID
Item
Sponsor-Defined Identifier
text
C0743223 (UMLS CUI [1,1])
C2347796 (UMLS CUI [1,2])
C0600091 (UMLS CUI [1,3])
DSSPID (SDTMIG 3.3)
C83250 (NCIt V19.10d)
TERM
Item
Reported Term for the Disposition Event
text
C2826302 (UMLS CUI [1,1])
C0743223 (UMLS CUI [1,2])
DSTERM (SDTMIG 3.3)
C74590 (NCIt V19.10d)
Item
Standardized Disposition Term
text
C0743223 (UMLS CUI [1,1])
C1442989 (UMLS CUI [1,2])
C0027365 (UMLS CUI [1,3])
DSDECOD (SDTMIG 3.3)
C89968 (NCIt V19.10d)
DECOD
Code List
Standardized Disposition Term
CL Item
ADVERSE EVENT (ADVERSE EVENT)
C0877248 (UMLS CUI-1)
C41331 (NCIt V19.10d)
CL Item
COMPLETED (COMPLETED)
C0205197 (UMLS CUI-1)
C25250 (NCIt V19.10d)
CL Item
Recurrent Disease (DISEASE RELAPSE)
C0277556 (UMLS CUI-1)
C38155 (NCIt V19.10d)
CL Item
FAILURE TO MEET CONTINUATION CRITERIA (FAILURE TO MEET CONTINUATION CRITERIA)
C4528356 (UMLS CUI-1)
C139236 (NCIt V19.10d)
CL Item
FAILURE TO MEET RANDOMIZATION CRITERIA (FAILURE TO MEET RANDOMIZATION CRITERIA)
C3642162 (UMLS CUI-1)
C105448 (NCIt V19.10d)
CL Item
LACK OF EFFICACY (LACK OF EFFICACY)
C0235828 (UMLS CUI-1)
C48226 (NCIt V19.10d)
CL Item
LOST TO FOLLOW-UP (LOST TO FOLLOW-UP)
C1302313 (UMLS CUI-1)
C48227 (NCIt V19.10d)
CL Item
Passed Screening But Not Needed; Qualified But Not Needed; Reserve, Not Used (MET ELIGIBILITY CRITERIA BUT NOT NEEDED)
C4726048 (UMLS CUI-1)
C150884 (NCIt V19.10d)
CL Item
NLCB (NO LONGER CLINICALLY BENEFITING)
C4744893 (UMLS CUI-1)
C156551 (NCIt V19.10d)
CL Item
NON-COMPLIANCE WITH NON-STUDY DEVICE (NON-COMPLIANCE WITH NON-STUDY DEVICE)
C4528360 (UMLS CUI-1)
C139240 (NCIt V19.10d)
CL Item
NON-COMPLIANCE WITH STUDY DEVICE (NON-COMPLIANCE WITH STUDY DEVICE)
C4528361 (UMLS CUI-1)
C139241 (NCIt V19.10d)
CL Item
NON-COMPLIANCE WITH STUDY DRUG (NON-COMPLIANCE WITH STUDY DRUG)
C1709261 (UMLS CUI-1)
C49631 (NCIt V19.10d)
CL Item
NON-COMPLIANCE WITH STUDY SCHEDULE (NON-COMPLIANCE WITH STUDY SCHEDULE)
C5205788 (UMLS CUI-1)
C161411 (NCIt V19.10d)
CL Item
OTHEROther (OTHEROther)
C0205394 (UMLS CUI-1)
C17649 (NCIt V19.10d)
CL Item
PHYSICIAN DECISION (PHYSICIAN DECISION)
C1709536 (UMLS CUI-1)
C48250 (NCIt V19.10d)
CL Item
PREGNANCY (PREGNANCY)
C0032961 (UMLS CUI-1)
C25742 (NCIt V19.10d)
CL Item
Disease Progression; Progressive Disease (PROGRESSIVE DISEASE)
C1335499 (UMLS CUI-1)
C35571 (NCIt V19.10d)
CL Item
PROTOCOL DEVIATION (PROTOCOL DEVIATION)
C1705236 (UMLS CUI-1)
C50996 (NCIt V19.10d)
CL Item
PROTOCOL VIOLATION (PROTOCOL VIOLATION)
C1709750 (UMLS CUI-1)
C142185 (NCIt V19.10d)
CL Item
PROTOCOL-SPECIFIED WITHDRAWAL CRITERION MET (PROTOCOL-SPECIFIED WITHDRAWAL CRITERION MET)
C4684540 (UMLS CUI-1)
C142349 (NCIt V19.10d)
CL Item
RANDOMIZED BY MISTAKE (RANDOMIZED BY MISTAKE)
C4528357 (UMLS CUI-1)
C139237 (NCIt V19.10d)
CL Item
RANDOMIZED BY MISTAKE WITH STUDY TREATMENT (RANDOMIZED BY MISTAKE WITH STUDY TREATMENT)
C4528358 (UMLS CUI-1)
C139238 (NCIt V19.10d)
CL Item
RANDOMIZED BY MISTAKE WITHOUT STUDY TREATMENT (RANDOMIZED BY MISTAKE WITHOUT STUDY TREATMENT)
C4528359 (UMLS CUI-1)
C139239 (NCIt V19.10d)
CL Item
RECOVERY (RECOVERY)
C2004454 (UMLS CUI-1)
C25746 (NCIt V19.10d)
CL Item
SCREEN FAILURE (SCREEN FAILURE)
C1710476 (UMLS CUI-1)
C49628 (NCIt V19.10d)
CL Item
SITE TERMINATED BY SPONSOR (SITE TERMINATED BY SPONSOR)
C3827772 (UMLS CUI-1)
C106576 (NCIt V19.10d)
CL Item
SPONSOR REQUEST (SPONSOR REQUEST)
C5205787 (UMLS CUI-1)
C161410 (NCIt V19.10d)
CL Item
STUDY TERMINATED BY SPONSOR (STUDY TERMINATED BY SPONSOR)
C1710224 (UMLS CUI-1)
C49632 (NCIt V19.10d)
CL Item
TECHNICAL PROBLEMS (TECHNICAL PROBLEMS)
C1710348 (UMLS CUI-1)
C49633 (NCIt V19.10d)
CL Item
WITHDRAWAL BY PARENT/GUARDIAN (WITHDRAWAL BY PARENT/GUARDIAN)
C3640719 (UMLS CUI-1)
C102355 (NCIt V19.10d)
CL Item
WITHDRAWAL BY SUBJECT (WITHDRAWAL BY SUBJECT)
C1710677 (UMLS CUI-1)
C49634 (NCIt V19.10d)
CL Item
Died (DEATH)
C0011065 (UMLS CUI-1)
C28554 (NCIt V19.10d)
CL Item
ELIGIBILITY CRITERIA MET (ELIGIBILITY CRITERIA MET)
PROTMLST (Comment:en)
C4329786 (UMLS CUI-1)
C132447 (NCIt V19.10d)
CL Item
ENTERED INTO TRIAL (ENTERED INTO TRIAL)
PROTMLST (Comment:en)
C5206987 (UMLS CUI-1)
C161417 (NCIt V19.10d)
CL Item
INFORMED ASSENT OBTAINED (INFORMED ASSENT OBTAINED)
PROTMLST (Comment:en)
C5205794 (UMLS CUI-1)
C161418 (NCIt V19.10d)
CL Item
INFORMED CONSENT OBTAINED (INFORMED CONSENT OBTAINED)
PROTMLST (Comment:en)
C0021430 (UMLS CUI-1)
C16735 (NCIt V19.10d)
CL Item
RANDOMIZED (RANDOMIZED)
PROTMLST (Comment:en)
C3815594 (UMLS CUI-1)
C114209 (NCIt V19.10d)
Item
Category for Disposition Event
text
C0683312 (UMLS CUI [1,1])
C0743223 (UMLS CUI [1,2])
DSCAT (SDTMIG 3.3)
C83245 (NCIt V19.10d)
CAT
Code List
Category for Disposition Event
CL Item
Disposition Event (DISPOSITION EVENT)
C2698907 (UMLS CUI-1)
C74590 (NCIt V19.10d)
CL Item
Other Event (OTHER EVENT)
C2698908 (UMLS CUI-1)
C74589 (NCIt V19.10d)
CL Item
Protocol Milestone (PROTOCOL MILESTONE)
C2698909 (UMLS CUI-1)
C74588 (NCIt V19.10d)
SCAT
Item
Subcategory for Disposition Event
text
C0743223 (UMLS CUI [1,1])
C0441471 (UMLS CUI [1,2])
C1515010 (UMLS CUI [1,3])
DSSCAT (SDTMIG 3.3)
C83248 (NCIt V19.10d)
Item
Epoch
text
C2347803 (UMLS CUI [1])
EPOCH (SDTMIG 3.3)
C71738 (NCIt V19.10d)
EPOCH
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])
C0743223 (UMLS CUI [1,2])
C1516698 (UMLS CUI [1,3])
DSDTC (SDTMIG 3.3)
C83246 (NCIt V19.10d)
STDTC
Item
Start Date/Time of Disposition Event
datetime
C0808070 (UMLS CUI [1,1])
C0743223 (UMLS CUI [1,2])
C1301880 (UMLS CUI [2,1])
C0743223 (UMLS CUI [2,2])
DSSTDTC (SDTMIG 3.3)
C83251 (NCIt V19.10d)
DY
Item
Study Day of Collection
datetime
C0743223 (UMLS CUI [1,1])
C2826182 (UMLS CUI [1,2])
C1516698 (UMLS CUI [1,3])
DSDY (SDTMIG 3.3)
C82437 (NCIt V19.10d)
C49576 (NCIt V19.10d-2)
STDY
Item
Study Day of Start of Disposition Event
text
C2826182 (UMLS CUI [1,1])
C0439659 (UMLS CUI [1,2])
C0743223 (UMLS CUI [1,3])
DSSTDY (SDTMIG 3.3)
C83252 (NCIt V19.10d)
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