0 Avaliações

ID

22797

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

12 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

    Intermittent Ropinirole in Restless Legs Syndrome (RLS) NCT00225862

    General Information
    Descrição

    General Information

    Alias
    UMLS CUI-1
    C1508263
    UMLS CUI-2
    C1955348
    UMLS CUI-3
    C0035258
    Subject Identifier
    Descrição

    Subject Identifier

    Tipo de dados

    text

    Alias
    UMLS CUI [1]
    C2348585
    Date of Beginning
    Descrição

    Date of Beginning

    Tipo de dados

    date

    Alias
    UMLS CUI [1]
    C0808070
    Date of End
    Descrição

    Date of End

    Tipo de dados

    date

    Alias
    UMLS CUI [1]
    C0806020
    RLS episode
    Descrição

    RLS episode

    Alias
    UMLS CUI-1
    C0035258
    UMLS CUI-2
    C0332189
    Date of RLS Episode
    Descrição

    Date of RLS Episode

    Tipo de dados

    date

    Alias
    UMLS CUI [1,1]
    C0011008
    UMLS CUI [1,2]
    C0035258
    UMLS CUI [1,3]
    C0332189
    Treatment of RLS Episode
    Descrição

    Treatment of RLS Episode

    Tipo de dados

    text

    Alias
    UMLS CUI [1,1]
    C0087111
    UMLS CUI [1,2]
    C0035258
    UMLS CUI [1,3]
    C0332189

    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
    C1508263 (UMLS CUI-1)
    C1955348 (UMLS CUI-2)
    C0035258 (UMLS CUI-3)
    Subject Identifier
    Item
    Subject Identifier
    text
    C2348585 (UMLS CUI [1])
    Date of Beginning
    Item
    Date of Beginning
    date
    C0808070 (UMLS CUI [1])
    Date of End
    Item
    Date of End
    date
    C0806020 (UMLS CUI [1])
    Item Group
    RLS episode
    C0035258 (UMLS CUI-1)
    C0332189 (UMLS CUI-2)
    Date of RLS Episode
    Item
    Date of RLS Episode
    date
    C0011008 (UMLS CUI [1,1])
    C0035258 (UMLS CUI [1,2])
    C0332189 (UMLS CUI [1,3])
    Item
    Treatment of RLS Episode
    text
    C0087111 (UMLS CUI [1,1])
    C0035258 (UMLS CUI [1,2])
    C0332189 (UMLS CUI [1,3])
    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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