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ID

22381

Descrição

Study ID: 100310 Clinical Study ID: RRL100310 Study Title: A 12-week, double-blind, placebo-controlled, parallel group study to assess the efficacy and safety of intermittent dosing of ropinirole in patients with Restless Legs Syndrome (RLS) Part 1: Visit 8 (Week 15) PRN Subject Diary Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00225862 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 3 Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: Modutab,ZIPEREVE,ZEPREVE,REPREVE,ADARTREL,REQUIP,Zygara; Zygara,ZIPEREVE,ZEPREVE,Requip Depot,REQUIP,REPREVE,Modutab,ADARTREL Study Indication: Restless Legs Syndrome More details on: https://clinicaltrials.gov/ct2/show/NCT00225862

Link

https://clinicaltrials.gov/ct2/show/NCT00225862

Palavras-chave

  1. 01/06/2017 01/06/2017 -
  2. 12/06/2017 12/06/2017 -
Transferido a

1 de junho de 2017

DOI

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Licença

Creative Commons BY-NC 3.0

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    Intermittent Ropinirole in Restless Legs Syndrome (RLS) NCT00225862 - Visit 8 (Week 15) PRN Subject Diary

    Intermittent Ropinirole in Restless Legs Syndrome (RLS) NCT00225862

    General Information
    Descrição

    General Information

    Subject Identifier
    Descrição

    Subject Identifier

    Tipo de dados

    text

    Date of Beginning
    Descrição

    Date of Beginning

    Tipo de dados

    date

    Date of End
    Descrição

    Date of End

    Tipo de dados

    date

    RLS episode
    Descrição

    RLS episode

    Date of RLS Episode
    Descrição

    Date of RLS Episode

    Tipo de dados

    date

    Treatment of RLS Episode
    Descrição

    Treatment of RLS Episode

    Tipo de dados

    text

    Similar models

    Intermittent Ropinirole in Restless Legs Syndrome (RLS) NCT00225862

    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de dados
    Alias
    Item Group
    General Information
    Subject Identifier
    Item
    Subject Identifier
    text
    Date of Beginning
    Item
    Date of Beginning
    date
    Date of End
    Item
    Date of End
    date
    Item Group
    RLS episode
    Date of RLS Episode
    Item
    Date of RLS Episode
    date
    Item
    Treatment of RLS Episode
    text
    Code List
    Treatment of RLS Episode
    CL Item
    RLS episode has been treated.  (1)
    CL Item
    RLS episode has not been treated. (2)

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