Final Exam NCT01539746

  1. StudyEvent: ODM
    1. Final Exam NCT01539746
Date of visit
Beschreibung

Date of visit

Alias
UMLS CUI-1
C1320303
Date of visit
Beschreibung

date of visit

Datentyp

date

Alias
UMLS CUI [1]
C1320303
Study completion
Beschreibung

Study completion

Alias
UMLS CUI-1
C2826674
Was the study completion according the protocol in regular way?
Beschreibung

Was the study completion according the protocol in regular way?

Datentyp

boolean

Alias
UMLS CUI [1,1]
C2826674
UMLS CUI [1,2]
C2348563
Termination of study participation
Beschreibung

Termination of study participation

Alias
UMLS CUI-1
C2348581
Date of study termination (in case of early termination of study participation)
Beschreibung

Date of study termination (in case of early termination of study participation)

Datentyp

date

Alias
UMLS CUI [1,1]
C2348581
UMLS CUI [1,2]
C0011008
Reason for early study termination
Beschreibung

Reason for early study termination

Datentyp

integer

Alias
UMLS CUI [1,1]
C1272707
UMLS CUI [1,2]
C2348581
UMLS CUI [1,3]
C1279919
Date of death
Beschreibung

Date of death

Datentyp

date

Alias
UMLS CUI [1]
C1148348
If applicable, please specify: Death due to
Beschreibung

If applicable, please specify: Death due to

Datentyp

integer

Alias
UMLS CUI [1]
C0007465
Date of last regular study visit?
Beschreibung

Date of last regular study visit?

Datentyp

date

Alias
UMLS CUI [1,1]
C0545082
UMLS CUI [1,2]
C1517741
UMLS CUI [1,3]
C0011008

Ähnliche Modelle

Final Exam NCT01539746

  1. StudyEvent: ODM
    1. Final Exam NCT01539746
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
Date of visit
C1320303 (UMLS CUI-1)
date of visit
Item
Date of visit
date
C1320303 (UMLS CUI [1])
Item Group
Study completion
C2826674 (UMLS CUI-1)
regular completion of study
Item
Was the study completion according the protocol in regular way?
boolean
C2826674 (UMLS CUI [1,1])
C2348563 (UMLS CUI [1,2])
Item Group
Termination of study participation
C2348581 (UMLS CUI-1)
date of study termination
Item
Date of study termination (in case of early termination of study participation)
date
C2348581 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item
Reason for early study termination
integer
C1272707 (UMLS CUI [1,1])
C2348581 (UMLS CUI [1,2])
C1279919 (UMLS CUI [1,3])
Code List
Reason for early study termination
CL Item
death (1)
C0011065 (UMLS CUI-1)
CL Item
withdrawal of informed consent (2)
C2349954 (UMLS CUI-1)
C0021430 (UMLS CUI-2)
CL Item
other reason (3)
C3840932 (UMLS CUI-1)
date of death
Item
Date of death
date
C1148348 (UMLS CUI [1])
Item
If applicable, please specify: Death due to
integer
C0007465 (UMLS CUI [1])
Code List
If applicable, please specify: Death due to
CL Item
primary disease (1)
C0277554 (UMLS CUI-1)
CL Item
(S)AE (2)
C1519255 (UMLS CUI-1)
C0877248 (UMLS CUI-3)
date of last visit
Item
Date of last regular study visit?
date
C0545082 (UMLS CUI [1,1])
C1517741 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])