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ID

22797

Beschreibung

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

Stichworte

  1. 01.06.17 01.06.17 -
  2. 12.06.17 12.06.17 -
Hochgeladen am

12. Juni 2017

DOI

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Lizenz

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
    Beschreibung

    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
    Beschreibung

    Subject Identifier

    Datentyp

    text

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

    Date of Beginning

    Datentyp

    date

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

    Date of End

    Datentyp

    date

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

    RLS episode

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

    Date of RLS Episode

    Datentyp

    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
    Beschreibung

    Treatment of RLS Episode

    Datentyp

    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

    Ähnliche Modelle

    Intermittent Ropinirole in Restless Legs Syndrome (RLS) NCT00225862

    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datentyp
    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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