0 Ratings
ID

22797

Description

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

Keywords

Versions (2)
  1. 6/1/17 6/1/17 -
  2. 6/12/17 6/12/17 -
Uploaded on

June 12, 2017

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License

Creative Commons BY-NC 3.0
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    Intermittent Ropinirole in Restless Legs Syndrome (RLS) NCT00225862

    English

    Intermittent Ropinirole in Restless Legs Syndrome (RLS) NCT00225862

    1 forms  
    General Information
    Description

    General Information

    Alias
    UMLS CUI-1
    C1508263 (General information section)
    LOINC
    MTHU015719
    UMLS CUI-2
    C1955348 (Patient Information)
    UMLS CUI-3
    C0035258 (Restless Legs Syndrome)
    SNOMED
    32914008
    Subject Identifier
    Description

    Subject Identifier

    Data type

    text

    Alias
    UMLS CUI [1]
    C2348585 (Clinical Trial Subject Unique Identifier)
    Date of Beginning
    Description

    Date of Beginning

    Data type

    date

    Alias
    UMLS CUI [1]
    C0808070 (Start Date)
    Date of End
    Description

    Date of End

    Data type

    date

    Alias
    UMLS CUI [1]
    C0806020 (End date)
    SNOMED
    454551000124105
    LOINC
    MTHU008302
    RLS episode
    Description

    RLS episode

    Alias
    UMLS CUI-1
    C0035258 (Restless Legs Syndrome)
    SNOMED
    32914008
    UMLS CUI-2
    C0332189 (Episode of)
    SNOMED
    263503000
    Date of RLS Episode
    Description

    Date of RLS Episode

    Data type

    date

    Alias
    UMLS CUI [1,1]
    C0011008 (Date in time)
    SNOMED
    410671006
    UMLS CUI [1,2]
    C0035258 (Restless Legs Syndrome)
    SNOMED
    32914008
    UMLS CUI [1,3]
    C0332189 (Episode of)
    SNOMED
    263503000
    Treatment of RLS Episode
    Description

    Treatment of RLS Episode

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C0087111 (Therapeutic procedure)
    SNOMED
    277132007
    LOINC
    LP21090-3
    UMLS CUI [1,2]
    C0035258 (Restless Legs Syndrome)
    SNOMED
    32914008
    UMLS CUI [1,3]
    C0332189 (Episode of)
    SNOMED
    263503000
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    Similar models

    Intermittent Ropinirole in Restless Legs Syndrome (RLS) NCT00225862

    1 forms
    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    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])
    Treatment of RLS Episode
    Code List
    Treatment of RLS Episode
    CL Item
    RLS episode has been treated.  (1)
    CL Item
    RLS episode has not been treated. (2)
    Back to the top of the page 

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