ID
42817
Beskrivning
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
Nyckelord
Versioner (4)
- 2018-02-22 2018-02-22 -
- 2018-02-24 2018-02-24 -
- 2018-02-25 2018-02-25 -
- 2021-09-17 2021-09-17 -
Rättsinnehavare
gsk
Uppladdad den
17 september 2021
DOI
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Licens
Creative Commons BY-NC 3.0
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Ropinirole Case Report Form GSK RRL100013
SERIOUS ADVERSE EVENT
Beskrivning
SERIOUS ADVERSE EVENTS
Beskrivning
SERIOUS ADVERSE EVENTS
Datatyp
text
Alias
- UMLS CUI [1]
- C1519255
Beskrivning
Start Date
Datatyp
date
Alias
- UMLS CUI [1]
- C0808070
Beskrivning
Start Time
Datatyp
time
Alias
- UMLS CUI [1]
- C1301880
Beskrivning
Outcome
Datatyp
text
Alias
- UMLS CUI [1]
- C1705586
Beskrivning
End Date
Datatyp
text
Alias
- UMLS CUI [1]
- C0806020
Beskrivning
End time
Datatyp
time
Alias
- UMLS CUI [1]
- C1522314
Beskrivning
Maximum Intensity
Datatyp
text
Alias
- UMLS CUI [1]
- C1710066
Beskrivning
Action Taken with Investigational Product(s) as a Result of the Serious AE
Datatyp
text
Alias
- UMLS CUI [1,1]
- C1704758
- UMLS CUI [1,2]
- C1519255
Beskrivning
Withdrawal
Datatyp
text
Alias
- UMLS CUI [1,1]
- C2349954
- UMLS CUI [1,2]
- C1519255
Beskrivning
Relationship to lnvestigational Product(s)
Datatyp
text
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C1522508
Beskrivning
Did the subject experience any serious adverse events during the study?
Datatyp
boolean
Alias
- UMLS CUI [1]
- C1519255
Similar models
SERIOUS ADVERSE EVENT
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
C1519255 (UMLS CUI-2)
(Comment:en)
C1519255 (UMLS CUI [1,2])
C1519255 (UMLS CUI [1,2])
C1522508 (UMLS CUI [1,2])