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ID

24663

Description

Study part: Assessment Of Rebound (RBND). A 52-Week, Open-Label Study to Assess the Long-Term Safety of Ropinirole Extended Release (XR) in Patients with Restless Legs Syndrome (RLS). Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Clinicaltrials.gov Identifier: NCT00355641. 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. Study ID: 101468/206. Clinical Study ID: 101468/206.

Keywords

  1. 8/12/17 8/12/17 -
Copyright Holder

GlaxoSmithKline

Uploaded on

August 12, 2017

DOI

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License

Creative Commons BY-NC 3.0

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    Assessment Of Rebound (RBND) Ropinirole Restless Legs Syndrom NCT00355641

    Assessment Of Rebound (RBND)

    ASSESSMENT OF REBOUND (RBND)
    Description

    ASSESSMENT OF REBOUND (RBND)

    Alias
    UMLS CUI-1
    C0220825
    1. RLS rebound experienced at end of dose?
    Description

    End of dose rebound, defined as a re-emergence of RLS symptoms in the early morning the day after taking the dose of RLS medication.

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0549262
    UMLS CUI [1,2]
    C0035258
    2. Assessor
    Description

    Assessor

    Data type

    text

    Alias
    UMLS CUI [1]
    C2646699

    Similar models

    Assessment Of Rebound (RBND)

    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    ASSESSMENT OF REBOUND (RBND)
    C0220825 (UMLS CUI-1)
    rebound RLS
    Item
    1. RLS rebound experienced at end of dose?
    boolean
    C0549262 (UMLS CUI [1,1])
    C0035258 (UMLS CUI [1,2])
    Item
    2. Assessor
    text
    C2646699 (UMLS CUI [1])
    Code List
    2. Assessor
    CL Item
    Investigator (Investigator)
    CL Item
    Health care professional or nurse (Health care professional or nurse)

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