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VX-950HPC3006 NCT01571583 Trial Completion

1 forms  
Trial completion
Description

Trial completion

did the subject experience any Adverse Events during the trial?
Description

if yes, please ensure that all Adverse Events are recorded on the Adverse Event form

Data type

boolean

Alias
UMLS CUI [1]
C0877248
did the subject take any concomitant medication during the trial?
Description

if yes, please ensure that all medications are recorded on the concomitant medication form

Data type

boolean

Alias
UMLS CUI [1]
C2347852
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Similar models

VX-950HPC3006 NCT01571583 Trial Completion

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Trial completion
adverse events during trial
Item
did the subject experience any Adverse Events during the trial?
boolean
C0877248 (UMLS CUI [1])
concomitant medication
Item
did the subject take any concomitant medication during the trial?
boolean
C2347852 (UMLS CUI [1])
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