ID

24665

Description

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.

Keywords

  1. 8/12/17 8/12/17 -
  2. 8/12/17 8/12/17 -
  3. 8/18/17 8/18/17 -
  4. 9/8/17 9/8/17 -
Uploaded on

August 12, 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
Description

General information

Protocol indentifier
Description

Protocol indentifier

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Subject Identifier
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Subject Identifier

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Alias
UMLS CUI [1]
C2348585
Visit date
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Visit date

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date

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Adverse events
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Adverse events

Adverse events
Description

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.

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

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C2348585 (UMLS CUI [1])
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date
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Adverse events
Adverse events
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