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ID
29055
Description
Ropinirole Case Report Form GSK RRL100013 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 (5)
- 10/5/17 10/5/17 -
- 2/22/18 2/22/18 -
- 2/22/18 2/22/18 -
- 2/22/18 2/22/18 -
- 9/17/21 9/17/21 -
Copyright Holder
gsk
Uploaded on
February 22, 2018
DOI
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License
Creative Commons BY-NC 3.0
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Ropinirole Case Report Form GSK RRL100013
Ropinirole Case Report Form GSK RRL100013
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Ropinirole Case Report Form GSK RRL100013
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Study Identifier
Item
STUDY NO.
text
C2826693 (UMLS CUI [1])
Subject No.
Item
Subject No.:
text
C2348585 (UMLS CUI [1])
Panel ID
Item
Panel ID:
integer
C0086373 (UMLS CUI [1])
Visit
Item
Visit:
integer
C1549755 (UMLS CUI [1])
Date
Item
Date:
date
C0011008 (UMLS CUI [1])
Prescribed or OTC medication
Item
Has the subject taken any prescribed medication within 14 days prior to first dosing day or any OTC medicine within 7 days before the first study day?
boolean
C3166216 (UMLS CUI [1])
C0013231 (UMLS CUI [2])
C0013231 (UMLS CUI [2])
DRUG NAME
Item
DRUG NAME
text
C2360065 (UMLS CUI [1])
Single Dose/Unit
Item
Single Dose/Unit
integer
C1960417 (UMLS CUI [1])
Frequency of this Dose
Item
Frequency of this Dose (e.g.BID, PR)
integer
C3476109 (UMLS CUI [1])
Route
Item
Route
text
C0013153 (UMLS CUI [1])
Indication
Item
Indication
text
C3146298 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
C0013227 (UMLS CUI [1,2])
Duration of therapy
Item
Duration of therapy
integer
C0444917 (UMLS CUI [1])
End Date
Item
End Date
date
C0013227 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
Continuing at end of study
Item
Continuing at end of study?
boolean
C1562611 (UMLS CUI [1])