ID

24665

Beskrivning

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.

Nyckelord

  1. 2017-08-12 2017-08-12 -
  2. 2017-08-12 2017-08-12 -
  3. 2017-08-18 2017-08-18 -
  4. 2017-09-08 2017-09-08 -
Uppladdad den

12 augusti 2017

DOI

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Licens

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
Beskrivning

General information

Protocol indentifier
Beskrivning

Protocol indentifier

Datatyp

text

Subject Identifier
Beskrivning

Subject Identifier

Datatyp

text

Alias
UMLS CUI [1]
C2348585
Visit date
Beskrivning

Visit date

Datatyp

date

Visit Description
Beskrivning

Visit Description

Datatyp

text

Adverse events
Beskrivning

Adverse events

Adverse events
Beskrivning

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.

Datatyp

text

Similar models

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

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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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