ID

24665

Beschrijving

Study ID: 101468/228 Clinical Study ID: 101468/228 Study Title:A two year Phase IIIb randomised, multicenter, double-blind, SINEMET controlled, parallel group, flexible dose study, to assess the effectiveness of controlled release ropinirole add-on therapy to L-dopa at increasing the time to onset of dyskinesia in Parkinson's disease subjects. Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00363727 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 3 Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: Zygara,ZIPEREVE,ZEPREVE,Requip Depot,REQUIP,REPREVE,Modutab,ADARTREL Study Indication : Dyskinesias; Parkinson Disease; Parkinson's Disease Study part: CGI-I Questionnaire.

Trefwoorden

  1. 12-08-17 12-08-17 -
  2. 12-08-17 12-08-17 -
  3. 18-08-17 18-08-17 -
  4. 08-09-17 08-09-17 -
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12 augustus 2017

DOI

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Creative Commons BY-NC 3.0

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CGI-I Questionnaire GSK study Dyskinesia in Parkinson's disease NCT00363727

CGI-I Questionnaire GSK study Dyskinesia in Parkinson's disease NCT00363727

General information
Beschrijving

General information

Protocol indentifier
Beschrijving

Protocol indentifier

Datatype

text

Subject Identifier
Beschrijving

Subject Identifier

Datatype

text

Alias
UMLS CUI [1]
C2348585
Visit date
Beschrijving

Visit date

Datatype

date

Visit Description
Beschrijving

Visit Description

Datatype

text

Adverse events
Beschrijving

Adverse events

Adverse events
Beschrijving

Record details of any new non-serious adverse events/serious adverse events observed or reported by the subject or any changes to ongoing non-serious adverse events in the appropriate Non-Serious Adverse Events/Serious Adverse Events section.

Datatype

text

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CGI-I Questionnaire GSK study Dyskinesia in Parkinson's disease NCT00363727

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
General information
Protocol indentifier
Item
Protocol indentifier
text
Subject Identifier
Item
Subject Identifier
text
C2348585 (UMLS CUI [1])
Visit date
Item
Visit date
date
Visit Description
Item
Visit Description
text
Item Group
Adverse events
Adverse events
Item
Adverse events
text

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