Status of treatment blind

STATUS OF TREATMENT BLIND
Beschreibung

STATUS OF TREATMENT BLIND

Alias
UMLS CUI-1
C0749659
UMLS CUI-2
C2347038
Study ID
Beschreibung

Study ID

Datentyp

text

Alias
UMLS CUI [1]
C2826693
Was the treatment blind broken during the study?
Beschreibung

Status of treatment blind

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0749659
UMLS CUI [1,2]
C2347038
Date blind broken
Beschreibung

date Blinded Clinical Study

Datentyp

date

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C2347038
Reason blind broken
Beschreibung

Complete Non-Serious Adverse Event, Serious Adverse Event and/or Investigational Product pages, as appropriate.

Datentyp

text

Alias
UMLS CUI [1,1]
C0392360
UMLS CUI [1,2]
C2347038
If other, please specify
Beschreibung

Other

Datentyp

text

Alias
UMLS CUI [1]
C0205394

Ähnliche Modelle

Status of treatment blind

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
STATUS OF TREATMENT BLIND
C0749659 (UMLS CUI-1)
C2347038 (UMLS CUI-2)
Study ID
Item
Study ID
text
C2826693 (UMLS CUI [1])
Status of treatment blind
Item
Was the treatment blind broken during the study?
boolean
C0749659 (UMLS CUI [1,1])
C2347038 (UMLS CUI [1,2])
date Blinded Clinical Study
Item
Date blind broken
date
C0011008 (UMLS CUI [1,1])
C2347038 (UMLS CUI [1,2])
Item
Reason blind broken
text
C0392360 (UMLS CUI [1,1])
C2347038 (UMLS CUI [1,2])
Code List
Reason blind broken
CL Item
Medical emergency requiring identification of investigational product for further treatment (Medical emergency requiring identification of investigational product for further treatment)
CL Item
Other, specify (Other, specify)
Other
Item
If other, please specify
text
C0205394 (UMLS CUI [1])