ID

24666

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: Adverse events.

Mots-clés

  1. 12/08/2017 12/08/2017 -
  2. 12/08/2017 12/08/2017 -
  3. 18/08/2017 18/08/2017 -
  4. 08/09/2017 08/09/2017 -
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12 août 2017

DOI

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Creative Commons BY-NC 3.0

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Adverse events GSK study Dyskinesia in Parkinson's disease NCT00363727

Adverse events GSK study Dyskinesia in Parkinson's disease NCT00363727

General information
Description

General information

Protocol indentifier
Description

Protocol indentifier

Type de données

text

Subject Identifier
Description

Subject Identifier

Type de données

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Alias
UMLS CUI [1]
C2348585
Visit date
Description

Visit date

Type de données

date

Visit Description
Description

Visit Description

Type de données

text

Adverse events
Description

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.

Type de données

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Adverse events GSK study Dyskinesia in Parkinson's disease NCT00363727

Name
Type
Description | Question | Decode (Coded Value)
Type de données
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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