ID

24666

Descrição

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.

Palavras-chave

  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 -
Transferido a

12 de agosto de 2017

DOI

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Licença

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
Descrição

General information

Protocol indentifier
Descrição

Protocol indentifier

Tipo de dados

text

Subject Identifier
Descrição

Subject Identifier

Tipo de dados

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Alias
UMLS CUI [1]
C2348585
Visit date
Descrição

Visit date

Tipo de dados

date

Visit Description
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Visit Description

Tipo de dados

text

Adverse events
Descrição

Adverse events

Adverse events
Descrição

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 dados

text

Similar models

Adverse events GSK study Dyskinesia in Parkinson's disease NCT00363727

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