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ID
25950
Description
Concomitant Medication Ropinirole Case Report Form GSK Study ID: 100013 Clinical Study ID: RRL100013 A 12-Week, Double-Blind, Placebo-Controlled, Twice-Daily Dosing Study to Assess the Efficacy and Safety of Ropinirole in Patients Suffering from Restless Legs Syndrome (RLS) Requiring Extended Treatment Coverage
Keywords
Versions (1)
- 10/1/17 10/1/17 -
Copyright Holder
gsk
Uploaded on
October 1, 2017
DOI
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License
Creative Commons BY-NC 3.0
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Concomitant Medication Ropinirole Case Report Form GSK RRL100013
Concomitant Medication Ropinirole Case Report Form GSK RRL100013
- StudyEvent: ODM
Similar models
Concomitant Medication Ropinirole Case Report Form GSK RRL100013
- StudyEvent: ODM
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Subject number
Item
Subject number
integer
C2348585 (UMLS CUI [1])
Concomitant Medication
Item
Are there any concomitant medication changes since the start of the study?
boolean
C2347852 (UMLS CUI [1])
Drug Name
Item
Drug Name
text
C0013227 (UMLS CUI [1])
Single dose
Item
Single dose/Unit
integer
C1960417 (UMLS CUI [1])
Frequency of this dose
Item
Frequency of this dose
integer
C2826654 (UMLS CUI [1])
Drug Administration Routes
Item
Drug Administration Routes
text
C0013153 (UMLS CUI [1])
Indication
Item
Indication
text
C3146298 (UMLS CUI [1])
Start Date and Time
Item
Start Date/Time
datetime
C3897500 (UMLS CUI [1])
End Date and Time
Item
End Date/Time
datetime
C3899266 (UMLS CUI [1])