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
NON-SERIOUS ADVERSE EVENT
Description
NON-SERIOUS ADVERSE EVENTS
Description
NON-SERIOUS ADVERSE EVENTS
Data type
text
Alias
- UMLS CUI [1]
- C1518404
Description
Start Date
Data type
date
Alias
- UMLS CUI [1]
- C0808070
Description
Start Time
Data type
time
Alias
- UMLS CUI [1]
- C1301880
Description
Outcome
Data type
text
Alias
- UMLS CUI [1]
- C1705586
Description
End Date
Data type
text
Alias
- UMLS CUI [1]
- C0806020
Description
End time
Data type
time
Alias
- UMLS CUI [1]
- C1522314
Description
Maximum Intensity
Data type
text
Alias
- UMLS CUI [1]
- C1710066
Description
Action Taken with Investigational Product(s) as a Result of the Non-Serious AE
Data type
text
Alias
- UMLS CUI [1,1]
- C1704758
- UMLS CUI [1,2]
- C1518404
Description
Withdrawal
Data type
text
Alias
- UMLS CUI [1,1]
- C2349954
- UMLS CUI [1,2]
- C1519255
Description
Relationship to lnvestigational Product(s)
Data type
text
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C1522508
Description
Did the subject experience any non-serious adverse events during the study?
Data type
boolean
Alias
- UMLS CUI [1]
- C1518404
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NON-SERIOUS ADVERSE EVENT
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C1519255 (UMLS CUI-2)
(Comment:en)
C1518404 (UMLS CUI [1,2])
C1519255 (UMLS CUI [1,2])
C1522508 (UMLS CUI [1,2])