English

Observation Class: Findings - Domain: Death Details

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
Death Details
Description

Death Details

Alias
SDTMIG v3.3
DD
UMLS CUI-1
C0011065
UMLS CUI-2
C1522508
NCIt V19.10d:
C95087
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): DD

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]
C0011065
UMLS CUI [1,2]
C1522508
UMLS CUI [1,3]
C2348184
SDTMIG 3.3
DDSEQ
NCIt V19.10d
C117543
Death Detail Assessment Short Name
Description

Role: Topic CDISC Notes (for domains) Description (for General Classes): Short name of the measurement, test, or examination described in DDTEST. It can be used as a column name when converting a dataset from a vertical to a horizontal format. The value in DDTESTCD cannot be longer than 8 characters, nor can it start with a number (e.g., "1TEST" is not valid). DDTESTCD cannot contain characters other than letters, numbers, or underscores. Examples: "PRCDTH", "SECDTH". Controlled Terms or Format (if applicable): (DTHDXCD), extensible

Data type

text

Alias
UMLS CUI [1,1]
C0011065
UMLS CUI [1,2]
C1522508
UMLS CUI [1,3]
C0392366
UMLS CUI [1,4]
C1806781
UMLS CUI [1,5]
C0027365
SDTMIG 3.3
DDTESTCD
NCIt V19.10d
C117544
Death Detail Assessment Name
Description

Role: Synonym Qualifier CDISC Notes (for domains) Description (for General Classes): Long name for DDTESTCD. The value in DDTEST cannot be longer than 40 characters. Examples: "Primary Cause of Death", "Secondary Cause of Death". Controlled Terms or Format (if applicable): (DTHDX), extensible

Data type

text

Alias
UMLS CUI [1,1]
C0011065
UMLS CUI [1,2]
C1522508
UMLS CUI [1,3]
C0392366
UMLS CUI [1,4]
C0027365
SDTMIG 3.3
DDTEST
NCIt V19.10d
C117545
Result or Finding as Collected
Description

Role: Result Qualifier CDISC Notes (for domains) Description (for General Classes): Result of the test defined in DDTEST, as originally received or collected. Controlled Terms or Format (if applicable): NA

Data type

text

Alias
UMLS CUI [1,1]
C0011065
UMLS CUI [1,2]
C1274040
UMLS CUI [1,3]
C0205313
SDTMIG 3.3
DDORRES
NCIt V19.10d
C117546
Character Result/Finding in Std Format
Description

Role: Result Qualifier CDISC Notes (for domains) Description (for General Classes): Contains the result or finding copied or derived from DDORRES in a standard format. Controlled Terms or Format (if applicable): NA

Data type

text

Alias
UMLS CUI [1,1]
C0011065
UMLS CUI [1,2]
C2350015
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1442989
UMLS CUI [1,5]
C1301627
SDTMIG 3.3
DDSTRESC
NCIt V19.10d
C117547
Result Category
Description

Role: Variable Qualifier CDISC Notes (for domains) Description (for General Classes): Used to categorize the result of a finding. Examples: "TREATMENT RELATED", "NONTREATMENT RELATED", "UNDETERMINED", "ACCIDENTAL". Controlled Terms or Format (if applicable): NA

Data type

text

Alias
UMLS CUI [1,1]
C0011065
UMLS CUI [1,2]
C1274040
UMLS CUI [1,3]
C0683312
SDTMIG 3.3
DDRESCAT
NCIt V19.10d
C102742
Evaluator
Description

Role: Record Qualifier CDISC Notes (for domains) Description (for General Classes): Role of the person who provided the evaluation. Controlled Terms or Format (if applicable): (EVAL), extensible

Data type

text

Alias
UMLS CUI [1,1]
C0011065
UMLS CUI [1,2]
C1707957
SDTMIG 3.3
DDEVAL
NCIt V19.10d
C117548
Date/Time of Collection
Description

Role: Timing CDISC Notes (for domains) Description (for General Classes): Date/time of collection of the diagnosis or other death assessment data in ISO 8601 format. This is not necessarily the date of death. Controlled Terms or Format (if applicable): ISO 8601

Data type

datetime

Alias
UMLS CUI [1,1]
C1264639
UMLS CUI [1,2]
C0011065
UMLS CUI [1,3]
C1522508
UMLS CUI [1,4]
C1516698
SDTMIG 3.3
DDDTC
NCIt V19.10d
C117549
Study Day of Collection
Description

Role: Timing CDISC Notes (for domains) Description (for General Classes): Study day of the collection, in integer days. The algorithm for calculations must be relative to the sponsor-defined RFSTDTC variable in the Demographics (DM) domain. Controlled Terms or Format (if applicable): NA

Data type

integer

Measurement units
  • d
Alias
UMLS CUI [1,1]
C2826182
UMLS CUI [1,2]
C0011065
UMLS CUI [1,3]
C1522508
UMLS CUI [1,4]
C1516698
SDTMIG 3.3
DDDY
NCIt V19.10d
C117550
d
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Similar models

Observation Class: Findings - Domain: Death Details

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
Death Details
DD (SDTMIG v3.3)
C0011065 (UMLS CUI-1)
C1522508 (UMLS CUI-2)
C95087 (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
C0011065 (UMLS CUI [1,1])
C1522508 (UMLS CUI [1,2])
C2348184 (UMLS CUI [1,3])
DDSEQ (SDTMIG 3.3)
C117543 (NCIt V19.10d)
Item
Death Detail Assessment Short Name
text
C0011065 (UMLS CUI [1,1])
C1522508 (UMLS CUI [1,2])
C0392366 (UMLS CUI [1,3])
C1806781 (UMLS CUI [1,4])
C0027365 (UMLS CUI [1,5])
DDTESTCD (SDTMIG 3.3)
C117544 (NCIt V19.10d)
TESTCD
Code List
Death Detail Assessment Short Name
CL Item
Age at Death (AGEDTH)
C1546180 (UMLS CUI-1)
C135383 (NCIt V19.10d)
CL Item
Autopsy Indicator (AUTOPIND)
C4525758 (UMLS CUI-1)
C135384 (NCIt V19.10d)
CL Item
Death Certificate Obtained Indicator (DTHCOIND)
C4525759 (UMLS CUI-1)
C135385 (NCIt V19.10d)
CL Item
Hospital Medical Record Obtained Ind; Hospital Medical Record Obtained Indicator (HMROIND)
C4525760 (UMLS CUI-1)
C135386 (NCIt V19.10d)
CL Item
Location of Death (LOCDTH)
C2924451 (UMLS CUI-1)
C124331 (NCIt V19.10d)
CL Item
Primary Cause of Death (PRCDTH)
C3262229 (UMLS CUI-1)
C99531 (NCIt V19.10d)
CL Item
Secondary Cause of Death (SECDTH)
C3262233 (UMLS CUI-1)
C116142 (NCIt V19.10d)
Item
Death Detail Assessment Name
text
C0011065 (UMLS CUI [1,1])
C1522508 (UMLS CUI [1,2])
C0392366 (UMLS CUI [1,3])
C0027365 (UMLS CUI [1,4])
DDTEST (SDTMIG 3.3)
C117545 (NCIt V19.10d)
TEST
Code List
Death Detail Assessment Name
CL Item
Age at Death (Age at Death)
C1546180 (UMLS CUI-1)
C135383 (NCIt V19.10d)
CL Item
Autopsy Indicator (Autopsy Indicator)
C4525758 (UMLS CUI-1)
C135384 (NCIt V19.10d)
CL Item
Death Certificate Obtained Indicator (Death Certificate Obtained Indicator)
C4525759 (UMLS CUI-1)
C135385 (NCIt V19.10d)
CL Item
Hospital Medical Record Obtained Ind; Hospital Medical Record Obtained Indicator (Hospital Medical Record Obtained Ind)
C4525760 (UMLS CUI-1)
C135386 (NCIt V19.10d)
CL Item
Location of Death (Location of Death)
C2924451 (UMLS CUI-1)
C124331 (NCIt V19.10d)
CL Item
Primary Cause of Death (Primary Cause of Death)
C3262229 (UMLS CUI-1)
C99531 (NCIt V19.10d)
CL Item
Secondary Cause of Death (Secondary Cause of Death)
C3262233 (UMLS CUI-1)
C116142 (NCIt V19.10d)
ORRES
Item
Result or Finding as Collected
text
C0011065 (UMLS CUI [1,1])
C1274040 (UMLS CUI [1,2])
C0205313 (UMLS CUI [1,3])
DDORRES (SDTMIG 3.3)
C117546 (NCIt V19.10d)
STRESC
Item
Character Result/Finding in Std Format
text
C0011065 (UMLS CUI [1,1])
C2350015 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1442989 (UMLS CUI [1,4])
C1301627 (UMLS CUI [1,5])
DDSTRESC (SDTMIG 3.3)
C117547 (NCIt V19.10d)
RESCAT
Item
Result Category
text
C0011065 (UMLS CUI [1,1])
C1274040 (UMLS CUI [1,2])
C0683312 (UMLS CUI [1,3])
DDRESCAT (SDTMIG 3.3)
C102742 (NCIt V19.10d)
Item
Evaluator
text
C0011065 (UMLS CUI [1,1])
C1707957 (UMLS CUI [1,2])
DDEVAL (SDTMIG 3.3)
C117548 (NCIt V19.10d)
EVALID
Code List
Evaluator
CL Item
ADJUDICATION COMMITTEE (ADJUDICATION COMMITTEE)
C2700368 (UMLS CUI-1)
C78726 (NCIt V19.10d)
CL Item
ADJUDICATOR (ADJUDICATOR)
C0401783 (UMLS CUI-1)
C96561 (NCIt V19.10d)
CL Item
Caregiver (CAREGIVER)
C0085537 (UMLS CUI-1)
C17445 (NCIt V19.10d)
CL Item
CHILD (CHILD)
C0680063 (UMLS CUI-1)
C42708 (NCIt V19.10d)
CL Item
Research Associate (CLINICAL RESEARCH ASSOCIATE)
C1516627 (UMLS CUI-1)
C25465 (NCIt V19.10d)
CL Item
CRC (CLINICAL RESEARCH COORDINATOR)
C1710220 (UMLS CUI-1)
C51811 (NCIt V19.10d)
CL Item
Clinical Study Sponsor; Sponsor; Study Sponsor (CLINICAL STUDY SPONSOR)
C2347796 (UMLS CUI-1)
C70793 (NCIt V19.10d)
CL Item
Domestic Partner (DOMESTIC PARTNER)
C1549111 (UMLS CUI-1)
C53262 (NCIt V19.10d)
CL Item
Family Member (FAMILY MEMBER)
C0086282 (UMLS CUI-1)
C41256 (NCIt V19.10d)
CL Item
FRIEND (FRIEND)
C0079382 (UMLS CUI-1)
C72884 (NCIt V19.10d)
CL Item
GUARDIAN (GUARDIAN)
C0023226 (UMLS CUI-1)
C51828 (NCIt V19.10d)
CL Item
HEALTH CARE PROFESSIONAL (HEALTH CARE PROFESSIONAL)
C1704312 (UMLS CUI-1)
C53287 (NCIt V19.10d)
CL Item
INDEPENDENT ASSESSOR (INDEPENDENT ASSESSOR)
C2697672 (UMLS CUI-1)
C78720 (NCIt V19.10d)
CL Item
INTERVIEWER (INTERVIEWER)
C0021821 (UMLS CUI-1)
C63759 (NCIt V19.10d)
CL Item
INVESTIGATOR (INVESTIGATOR)
C0035173 (UMLS CUI-1)
C25936 (NCIt V19.10d)
CL Item
PARENT (PARENT)
C0030551 (UMLS CUI-1)
C42709 (NCIt V19.10d)
CL Item
PROXY (PROXY)
C3897813 (UMLS CUI-1)
C119264 (NCIt V19.10d)
CL Item
SIBLING (SIBLING)
C0037047 (UMLS CUI-1)
C25204 (NCIt V19.10d)
CL Item
SIGNIFICANT OTHER (SIGNIFICANT OTHER)
C0682323 (UMLS CUI-1)
C119265 (NCIt V19.10d)
CL Item
Spouse (SPOUSE)
C0162409 (UMLS CUI-1)
C62649 (NCIt V19.10d)
CL Item
STUDY SUBJECT (STUDY SUBJECT)
C0681850 (UMLS CUI-1)
C41189 (NCIt V19.10d)
CL Item
VENDOR (VENDOR)
C0042462 (UMLS CUI-1)
C68608 (NCIt V19.10d)
DTC
Item
Date/Time of Collection
datetime
C1264639 (UMLS CUI [1,1])
C0011065 (UMLS CUI [1,2])
C1522508 (UMLS CUI [1,3])
C1516698 (UMLS CUI [1,4])
DDDTC (SDTMIG 3.3)
C117549 (NCIt V19.10d)
DY
Item
Study Day of Collection
integer
C2826182 (UMLS CUI [1,1])
C0011065 (UMLS CUI [1,2])
C1522508 (UMLS CUI [1,3])
C1516698 (UMLS CUI [1,4])
DDDY (SDTMIG 3.3)
C117550 (NCIt V19.10d)
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