1. StudyEvent: ODM
    1. Death
Administrative Data
Beschreibung

Administrative Data

Alias
UMLS CUI-1
C1320722
Subject Identifier
Beschreibung

Clinical Trial Subject Unique Identifier

Datentyp

integer

Alias
UMLS CUI [1]
C2348585
Death
Beschreibung

Death

Alias
UMLS CUI-1
C0011065
Date of Death
Beschreibung

Date of death

Datentyp

date

Alias
UMLS CUI [1]
C1148348
Indicate the primary cause of death.
Beschreibung

Primary Cause of Death

Datentyp

text

Alias
UMLS CUI [1]
C3262229
Specify
Beschreibung

Primary Cause of Death

Datentyp

text

Alias
UMLS CUI [1]
C3262229

Ähnliche Modelle

  1. StudyEvent: ODM
    1. Death
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
Administrative Data
C1320722 (UMLS CUI-1)
Clinical Trial Subject Unique Identifier
Item
Subject Identifier
integer
C2348585 (UMLS CUI [1])
Item Group
Death
C0011065 (UMLS CUI-1)
Date of death
Item
Date of Death
date
C1148348 (UMLS CUI [1])
Item
Indicate the primary cause of death.
text
C3262229 (UMLS CUI [1])
Code List
Indicate the primary cause of death.
CL Item
Disease under study (1)
CL Item
Haematologic toxicity (2)
CL Item
Non-haematologic toxicity (3)
CL Item
Other, specify (4)
Primary Cause of Death
Item
Specify
text
C3262229 (UMLS CUI [1])