English

Observation Class: Events - Domain: Healthcare Encounters

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
Healthcare Encounters
Description

Healthcare Encounters

Alias
SDTMIG v3.3
HO
UMLS CUI-1
C0086388
UMLS CUI-2
C0545082
NCIt V19.10d:
C117757
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): HO

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]
C0086388
UMLS CUI [1,2]
C0545082
UMLS CUI [1,3]
C2348184
SDTMIG 3.3
HOSEQ
NCIt V19.10d
C124001
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]
C0086388
UMLS CUI [1,2]
C0545082
UMLS CUI [1,3]
C0441833
UMLS CUI [1,4]
C0600091
SDTMIG 3.3
HOGRPID
NCIt V19.10d
C123971
Reference ID
Description

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

Data type

text

Alias
UMLS CUI [1,1]
C0086388
UMLS CUI [1,2]
C0545082
UMLS CUI [1,3]
C2826265
SDTMIG 3.3
HOREFID
NCIt V19.10d
C123995
Sponsor-Defined Identifier
Description

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

Data type

text

Alias
UMLS CUI [1,1]
C0086388
UMLS CUI [1,2]
C0545082
UMLS CUI [1,3]
C2347796
UMLS CUI [1,4]
C0600091
SDTMIG 3.3
HOSPID
NCIt V19.10d
C124004
Healthcare Encounter Term
Description

Role: Topic CDISC Notes (for domains) Description (for General Classes): Verbatim or preprinted CRF term for the healthcare encounter. Controlled Terms or Format (if applicable): NA

Data type

text

Alias
UMLS CUI [1,1]
C0086388
UMLS CUI [1,2]
C0545082
UMLS CUI [1,3]
C0027365
SDTMIG 3.3
HOTERM
NCIt V19.10d
C124023
Dictionary-Derived Term
Description

Role: Synonym Qualifier CDISC Notes (for domains) Description (for General Classes): Dictionary or sponsor-defined derived text description of HOTERM or the modified topic variable (HOMODIFY). Controlled Terms or Format (if applicable): NA

Data type

text

Alias
UMLS CUI [1,1]
C0086388
UMLS CUI [1,2]
C0545082
UMLS CUI [1,3]
C2826605
SDTMIG 3.3
HODECOD
NCIt V19.10d
C123944
Category for Healthcare Encounter
Description

Role: Grouping Qualifier CDISC Notes (for domains) Description (for General Classes): Used to define a category of topic-related values. Controlled Terms or Format (if applicable): NA

Data type

text

Alias
UMLS CUI [1,1]
C0683312
UMLS CUI [1,2]
C0086388
UMLS CUI [1,3]
C0545082
SDTMIG 3.3
HOCAT
NCIt V19.10d
C123940
Subcategory for Healthcare Encounter
Description

Role: Grouping Qualifier CDISC Notes (for domains) Description (for General Classes): A further categorization of HOCAT values. Controlled Terms or Format (if applicable): NA

Data type

text

Alias
UMLS CUI [1,1]
C0086388
UMLS CUI [1,2]
C0545082
UMLS CUI [1,3]
C1515010
SDTMIG 3.3
HOSCAT
NCIt V19.10d
C123999
Pre-Specified Healthcare Encounter
Description

Role: Variable Qualifier CDISC Notes (for domains) Description (for General Classes): 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). Controlled Terms or Format (if applicable): (NY), not extensible

Data type

text

Alias
UMLS CUI [1,1]
C0086388
UMLS CUI [1,2]
C0545082
UMLS CUI [1,3]
C2826245
SDTMIG 3.3
HOPRESP
NCIt V19.10d
C123989
Healthcare Encounter Occurrence
Description

Role: Record Qualifier CDISC Notes (for domains) Description (for General Classes): 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. Controlled Terms or Format (if applicable): (NY), not extensible

Data type

text

Alias
UMLS CUI [1,1]
C0086388
UMLS CUI [1,2]
C0545082
UMLS CUI [1,3]
C2745955
SDTMIG 3.3
HOOCCUR
NCIt V19.10d
C123982
Completion Status
Description

Role: Record Qualifier CDISC Notes (for domains) Description (for General Classes): The status indicates that the pre-specified question was not answered. Controlled Terms or Format (if applicable): (ND)

Data type

text

Alias
UMLS CUI [1,1]
C0086388
UMLS CUI [1,2]
C0545082
UMLS CUI [1,3]
C0805732
UMLS CUI [1,4]
C1522634
SDTMIG 3.3
HOSTAT
NCIt V19.10d
C124007
Reason Healthcare Encounter Not Done
Description

Role: Record Qualifier CDISC Notes (for domains) Description (for General Classes): Describes the reason data for a pre-specified event was not collected. Used in conjunction with HOSTAT when value is "NOT DONE". Controlled Terms or Format (if applicable): NA

Data type

text

Alias
UMLS CUI [1,1]
C0086388
UMLS CUI [1,2]
C0545082
UMLS CUI [1,3]
C2826287
SDTMIG 3.3
HOREASND
NCIt V19.10d
C123993
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. 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 start date/time of the healthcare encounter. Examples: "SCREENING", "TREATMENT", "FOLLOW-UP". Controlled Terms or Format (if applicable): (EPOCH)

Data type

text

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

Role: Timing CDISC Notes (for domains) Description (for General Classes): Collection date and time of the healthcare encounter. Controlled Terms or Format (if applicable): ISO 8601

Data type

datetime

Alias
UMLS CUI [1,1]
C1264639
UMLS CUI [1,2]
C0086388
UMLS CUI [1,3]
C0545082
UMLS CUI [1,4]
C1516698
SDTMIG 3.3
HODTC
NCIt V19.10d
C123947
Start Date/Time of Healthcare Encounter
Description

Role: Timing CDISC Notes (for domains) Description (for General Classes): Start date/time of the healthcare encounter (e.g., date of admission). Controlled Terms or Format (if applicable): ISO 8601

Data type

datetime

Alias
UMLS CUI [1,1]
C0808070
UMLS CUI [1,2]
C0086388
UMLS CUI [1,3]
C0545082
UMLS CUI [2,1]
C1301880
UMLS CUI [2,2]
C0086388
UMLS CUI [2,3]
C0545082
SDTMIG 3.3
HOSTDTC
NCIt V19.10d
C124009
End Date/Time of Healthcare Encounter
Description

Role: Timing CDISC Notes (for domains) Description (for General Classes): End date/time of the healthcare encounter (date of discharge). Controlled Terms or Format (if applicable): ISO 8601

Data type

datetime

Alias
UMLS CUI [1,1]
C0806020
UMLS CUI [1,2]
C0086388
UMLS CUI [1,3]
C0545082
UMLS CUI [2,1]
C1522314
UMLS CUI [2,2]
C0086388
UMLS CUI [2,3]
C0545082
SDTMIG 3.3
HOENDTC
NCIt V19.10d
C123956
Study Day of Event Collection
Description

Role: Timing CDISC Notes (for domains) Description (for General Classes): Study day of event collection 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]
C0086388
UMLS CUI [1,3]
C0545082
UMLS CUI [1,4]
C1516698
SDTMIG 3.3
HODY
NCIt V19.10d
C123951
Study Day of Start of Encounter
Description

Role: Timing CDISC Notes (for domains) Description (for General Classes): Study day of the start of the healthcare encounter 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]
C0086388
UMLS CUI [1,4]
C0545082
SDTMIG 3.3
HOSTDY
NCIt V19.10d
C124010
Study Day of End of Healthcare Encounter
Description

Role: Timing CDISC Notes (for domains) Description (for General Classes): Study day of the end of the healthcare encounter 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]
C0444930
UMLS CUI [1,3]
C0086388
UMLS CUI [1,4]
C0545082
SDTMIG 3.3
HOENDY
NCIt V19.10d
C123959
Duration of Healthcare Encounter
Description

Role: Timing CDISC Notes (for domains) Description (for General Classes): 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). Controlled Terms or Format (if applicable): ISO 8601

Data type

durationDatetime

Alias
UMLS CUI [1,1]
C0449238
UMLS CUI [1,2]
C0086388
UMLS CUI [1,3]
C0545082
SDTMIG 3.3
HODUR
NCIt V19.10d
C123949
Start Relative to Reference Time Point
Description

Role: Timing CDISC Notes (for domains) Description (for General Classes): Identifies the start of the observation as being before or after the sponsor-defined reference time point defined by variable --STTPT. Not all values of the codelist are allowable for this variable. See Section 4.4.7, Use of Relative Timing Variables. Controlled Terms or Format (if applicable): (STENRF), not extensible

Data type

text

Alias
UMLS CUI [1,1]
C0086388
UMLS CUI [1,2]
C0545082
UMLS CUI [1,3]
C0439659
UMLS CUI [1,4]
C0439564
UMLS CUI [1,5]
C1709877
UMLS CUI [1,6]
C2348792
SDTMIG 3.3
HOSTRTPT
NCIt V19.10d
C124021
Start Reference Time Point
Description

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

Data type

text

Alias
UMLS CUI [1,1]
C0086388
UMLS CUI [1,2]
C0545082
UMLS CUI [1,3]
C0439659
UMLS CUI [1,4]
C1709877
UMLS CUI [1,5]
C2348792
SDTMIG 3.3
HOSTTPT
NCIt V19.10d
C124022
End Relative to Reference Time Point
Description

Role: Timing CDISC Notes (for domains) Description (for General Classes): Identifies the end of the event as being before or after the reference time point defined by variable HOENTPT. Not all values of the codelist are allowable for this variable. See Section 4.4.7, Use of Relative Timing Variables. Controlled Terms or Format (if applicable): (STENRF), not extensible

Data type

text

Alias
UMLS CUI [1,1]
C0086388
UMLS CUI [1,2]
C0545082
UMLS CUI [1,3]
C0439659
UMLS CUI [1,4]
C0439564
UMLS CUI [1,5]
C1709877
UMLS CUI [1,6]
C2348792
SDTMIG 3.3
HOENRTPT
NCIt V19.10d
C123965
End Reference Time Point
Description

Role: Timing CDISC Notes (for domains) Description (for General Classes): Description or date/time in ISO 8601 character format of the reference point referred to by HOENRTPT. Examples: "2003-12-25" or "VISIT 2". Controlled Terms or Format (if applicable): NA

Data type

text

Alias
UMLS CUI [1,1]
C0086388
UMLS CUI [1,2]
C0545082
UMLS CUI [1,3]
C0439659
UMLS CUI [1,4]
C1709877
UMLS CUI [1,5]
C2348792
SDTMIG 3.3
HOENTPT
NCIt V19.10d
C123966
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Similar models

Observation Class: Events - Domain: Healthcare Encounters

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
Healthcare Encounters
HO (SDTMIG v3.3)
C0086388 (UMLS CUI-1)
C0545082 (UMLS CUI-2)
C117757 (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)
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
C0086388 (UMLS CUI [1,1])
C0545082 (UMLS CUI [1,2])
C2348184 (UMLS CUI [1,3])
HOSEQ (SDTMIG 3.3)
C124001 (NCIt V19.10d)
GRPID
Item
Group ID
text
C0086388 (UMLS CUI [1,1])
C0545082 (UMLS CUI [1,2])
C0441833 (UMLS CUI [1,3])
C0600091 (UMLS CUI [1,4])
HOGRPID (SDTMIG 3.3)
C123971 (NCIt V19.10d)
REFID
Item
Reference ID
text
C0086388 (UMLS CUI [1,1])
C0545082 (UMLS CUI [1,2])
C2826265 (UMLS CUI [1,3])
HOREFID (SDTMIG 3.3)
C123995 (NCIt V19.10d)
SPID
Item
Sponsor-Defined Identifier
text
C0086388 (UMLS CUI [1,1])
C0545082 (UMLS CUI [1,2])
C2347796 (UMLS CUI [1,3])
C0600091 (UMLS CUI [1,4])
HOSPID (SDTMIG 3.3)
C124004 (NCIt V19.10d)
TERM
Item
Healthcare Encounter Term
text
C0086388 (UMLS CUI [1,1])
C0545082 (UMLS CUI [1,2])
C0027365 (UMLS CUI [1,3])
HOTERM (SDTMIG 3.3)
C124023 (NCIt V19.10d)
DECOD
Item
Dictionary-Derived Term
text
C0086388 (UMLS CUI [1,1])
C0545082 (UMLS CUI [1,2])
C2826605 (UMLS CUI [1,3])
HODECOD (SDTMIG 3.3)
C123944 (NCIt V19.10d)
CAT
Item
Category for Healthcare Encounter
text
C0683312 (UMLS CUI [1,1])
C0086388 (UMLS CUI [1,2])
C0545082 (UMLS CUI [1,3])
HOCAT (SDTMIG 3.3)
C123940 (NCIt V19.10d)
SCAT
Item
Subcategory for Healthcare Encounter
text
C0086388 (UMLS CUI [1,1])
C0545082 (UMLS CUI [1,2])
C1515010 (UMLS CUI [1,3])
HOSCAT (SDTMIG 3.3)
C123999 (NCIt V19.10d)
Item
Pre-Specified Healthcare Encounter
text
C0086388 (UMLS CUI [1,1])
C0545082 (UMLS CUI [1,2])
C2826245 (UMLS CUI [1,3])
HOPRESP (SDTMIG 3.3)
C123989 (NCIt V19.10d)
DTHFL
Code List
Pre-Specified Healthcare Encounter
CL Item
No (N)
CL Item
NA; Not Applicable (NA)
CL Item
U; UNK; Unknown (U)
CL Item
Yes (Y)
Item
Healthcare Encounter Occurrence
text
C0086388 (UMLS CUI [1,1])
C0545082 (UMLS CUI [1,2])
C2745955 (UMLS CUI [1,3])
HOOCCUR (SDTMIG 3.3)
C123982 (NCIt V19.10d)
DTHFL
Code List
Healthcare Encounter Occurrence
CL Item
No (N)
CL Item
NA; Not Applicable (NA)
CL Item
U; UNK; Unknown (U)
CL Item
Yes (Y)
STAT
Item
Completion Status
text
C0086388 (UMLS CUI [1,1])
C0545082 (UMLS CUI [1,2])
C0805732 (UMLS CUI [1,3])
C1522634 (UMLS CUI [1,4])
HOSTAT (SDTMIG 3.3)
C124007 (NCIt V19.10d)
REASND
Item
Reason Healthcare Encounter Not Done
text
C0086388 (UMLS CUI [1,1])
C0545082 (UMLS CUI [1,2])
C2826287 (UMLS CUI [1,3])
HOREASND (SDTMIG 3.3)
C123993 (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)
EPOCH
Code List
Epoch
CL Item
BASELINE  (BASELINE )
CL Item
BLINDED TREATMENT  (BLINDED TREATMENT )
CL Item
Continuation Phase (CONTINUATION TREATMENT)
CL Item
FOLLOW-UP  (FOLLOW-UP )
CL Item
Induction Phase; Intensive Phase (INDUCTION TREATMENT)
CL Item
LONG-TERM FOLLOW-UP  (LONG-TERM FOLLOW-UP )
CL Item
OPEN LABEL TREATMENT  (OPEN LABEL TREATMENT )
CL Item
RUN-IN  (RUN-IN )
CL Item
SCREENING  (SCREENING )
CL Item
TREATMENT  (TREATMENT )
CL Item
WASHOUT  (WASHOUT )
DTC
Item
Date/Time of Event Collection
datetime
C1264639 (UMLS CUI [1,1])
C0086388 (UMLS CUI [1,2])
C0545082 (UMLS CUI [1,3])
C1516698 (UMLS CUI [1,4])
HODTC (SDTMIG 3.3)
C123947 (NCIt V19.10d)
STDTC
Item
Start Date/Time of Healthcare Encounter
datetime
C0808070 (UMLS CUI [1,1])
C0086388 (UMLS CUI [1,2])
C0545082 (UMLS CUI [1,3])
C1301880 (UMLS CUI [2,1])
C0086388 (UMLS CUI [2,2])
C0545082 (UMLS CUI [2,3])
HOSTDTC (SDTMIG 3.3)
C124009 (NCIt V19.10d)
ENDTC
Item
End Date/Time of Healthcare Encounter
datetime
C0806020 (UMLS CUI [1,1])
C0086388 (UMLS CUI [1,2])
C0545082 (UMLS CUI [1,3])
C1522314 (UMLS CUI [2,1])
C0086388 (UMLS CUI [2,2])
C0545082 (UMLS CUI [2,3])
HOENDTC (SDTMIG 3.3)
C123956 (NCIt V19.10d)
DY
Item
Study Day of Event Collection
text
C2826182 (UMLS CUI [1,1])
C0086388 (UMLS CUI [1,2])
C0545082 (UMLS CUI [1,3])
C1516698 (UMLS CUI [1,4])
HODY (SDTMIG 3.3)
C123951 (NCIt V19.10d)
STDY
Item
Study Day of Start of Encounter
text
C2826182 (UMLS CUI [1,1])
C0439659 (UMLS CUI [1,2])
C0086388 (UMLS CUI [1,3])
C0545082 (UMLS CUI [1,4])
HOSTDY (SDTMIG 3.3)
C124010 (NCIt V19.10d)
ENDY
Item
Study Day of End of Healthcare Encounter
text
C2826182 (UMLS CUI [1,1])
C0444930 (UMLS CUI [1,2])
C0086388 (UMLS CUI [1,3])
C0545082 (UMLS CUI [1,4])
HOENDY (SDTMIG 3.3)
C123959 (NCIt V19.10d)
DUR
Item
Duration of Healthcare Encounter
durationDatetime
C0449238 (UMLS CUI [1,1])
C0086388 (UMLS CUI [1,2])
C0545082 (UMLS CUI [1,3])
HODUR (SDTMIG 3.3)
C123949 (NCIt V19.10d)
Item
Start Relative to Reference Time Point
text
C0086388 (UMLS CUI [1,1])
C0545082 (UMLS CUI [1,2])
C0439659 (UMLS CUI [1,3])
C0439564 (UMLS CUI [1,4])
C1709877 (UMLS CUI [1,5])
C2348792 (UMLS CUI [1,6])
HOSTRTPT (SDTMIG 3.3)
C124021 (NCIt V19.10d)
STRF
Code List
Start Relative to Reference Time Point
CL Item
AFTER  (AFTER )
CL Item
BEFORE  (BEFORE )
CL Item
COINCItDENT  (COINCItDENT )
CL Item
DURING  (DURING )
CL Item
DURING/AFTER  (DURING/AFTER )
CL Item
Continuous (ONGOING)
CL Item
U; UNK; Unknown (UNKNOWN)
STTPT
Item
Start Reference Time Point
text
C0086388 (UMLS CUI [1,1])
C0545082 (UMLS CUI [1,2])
C0439659 (UMLS CUI [1,3])
C1709877 (UMLS CUI [1,4])
C2348792 (UMLS CUI [1,5])
HOSTTPT (SDTMIG 3.3)
C124022 (NCIt V19.10d)
Item
End Relative to Reference Time Point
text
C0086388 (UMLS CUI [1,1])
C0545082 (UMLS CUI [1,2])
C0439659 (UMLS CUI [1,3])
C0439564 (UMLS CUI [1,4])
C1709877 (UMLS CUI [1,5])
C2348792 (UMLS CUI [1,6])
HOENRTPT (SDTMIG 3.3)
C123965 (NCIt V19.10d)
STRF
Code List
End Relative to Reference Time Point
CL Item
AFTER  (AFTER )
CL Item
BEFORE  (BEFORE )
CL Item
COINCItDENT  (COINCItDENT )
CL Item
DURING  (DURING )
CL Item
DURING/AFTER  (DURING/AFTER )
CL Item
Continuous (ONGOING)
CL Item
U; UNK; Unknown (UNKNOWN)
ENTPT
Item
End Reference Time Point
text
C0086388 (UMLS CUI [1,1])
C0545082 (UMLS CUI [1,2])
C0439659 (UMLS CUI [1,3])
C1709877 (UMLS CUI [1,4])
C2348792 (UMLS CUI [1,5])
HOENTPT (SDTMIG 3.3)
C123966 (NCIt V19.10d)
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