0 Evaluaciones

ID

22381

Descripción

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

Palabras clave

  1. 1/6/17 1/6/17 -
  2. 12/6/17 12/6/17 -
Subido en

1 de junio de 2017

DOI

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Licencia

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
    Descripción

    General Information

    Subject Identifier
    Descripción

    Subject Identifier

    Tipo de datos

    text

    Date of Beginning
    Descripción

    Date of Beginning

    Tipo de datos

    date

    Date of End
    Descripción

    Date of End

    Tipo de datos

    date

    RLS episode
    Descripción

    RLS episode

    Date of RLS Episode
    Descripción

    Date of RLS Episode

    Tipo de datos

    date

    Treatment of RLS Episode
    Descripción

    Treatment of RLS Episode

    Tipo de datos

    text

    Similar models

    Intermittent Ropinirole in Restless Legs Syndrome (RLS) NCT00225862

    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de datos
    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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