ID

24666

Descripción

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.

Palabras clave

  1. 12/8/17 12/8/17 -
  2. 12/8/17 12/8/17 -
  3. 18/8/17 18/8/17 -
  4. 8/9/17 8/9/17 -
Subido en

12 de agosto de 2017

DOI

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Licencia

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
Descripción

General information

Protocol indentifier
Descripción

Protocol indentifier

Tipo de datos

text

Subject Identifier
Descripción

Subject Identifier

Tipo de datos

text

Alias
UMLS CUI [1]
C2348585
Visit date
Descripción

Visit date

Tipo de datos

date

Visit Description
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Visit Description

Tipo de datos

text

Adverse events
Descripción

Adverse events

Adverse events
Descripción

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.

Tipo de datos

text

Similar models

Adverse events GSK study Dyskinesia in Parkinson's disease NCT00363727

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
General information
Protocol indentifier
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Protocol indentifier
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Subject Identifier
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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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