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ID

40776

Description

Study ID: 101468/218 Clinical Study ID: SKF-101468/218 Study Title:A Single-Blind, Randomised, Placebo-Controlled, Parallel-Group, Multicentre, Phase IIa Study to Determine the Pharmacokinetics and Tolerability of Ropinirole in Patients Suffering from Restless Legs Syndrome (RLS) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Sponsor: GlaxoSmithKline Phase: phase 2 Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: requip Study Indication: Restless Legs Syndrome

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Versions (1)
  1. 5/11/20 5/11/20 -
Copyright Holder

GlaxoSmithKline

Uploaded on

May 11, 2020

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Creative Commons BY-NC 4.0
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    Pharmacokinetics and Tolerability of Ropinirole in Patients Suffering from Restless Legs Syndrome 101468/218

    English

    Return of Study Medication

    1 forms  
    Administrative
    Description

    Administrative

    Alias
    UMLS CUI-1
    C1320722
    Subject Number
    Description

    Subject Number

    Data type

    text

    Alias
    UMLS CUI [1]
    C2348585
    Centre Number
    Description

    Centre Number

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C0600091
    UMLS CUI [1,2]
    C0019994
    Visit Date
    Description

    Visit Date

    Data type

    date

    Alias
    UMLS CUI [1]
    C1320303
    Return of Study Medication
    Description

    Return of Study Medication

    Alias
    UMLS CUI-1
    C2826299
    Number of Tablets returned
    Description

    Number of Tablets returned

    Data type

    integer

    Alias
    UMLS CUI [1,1]
    C2699071
    UMLS CUI [1,2]
    C0039225
    Return of Study Medication - Comments
    Description

    Return of Study Medication - Comments

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C2826299
    UMLS CUI [1,2]
    C0947611
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    Similar models

    Return of Study Medication

    1 forms
    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    Administrative
    C1320722 (UMLS CUI-1)
    Subject Number
    Item
    Subject Number
    text
    C2348585 (UMLS CUI [1])
    Centre Number
    Item
    Centre Number
    text
    C0600091 (UMLS CUI [1,1])
    C0019994 (UMLS CUI [1,2])
    Visit Date
    Item
    Visit Date
    date
    C1320303 (UMLS CUI [1])
    Item Group
    Return of Study Medication
    C2826299 (UMLS CUI-1)
    Number of Tablets returned
    Item
    Number of Tablets returned
    integer
    C2699071 (UMLS CUI [1,1])
    C0039225 (UMLS CUI [1,2])
    Return of Study Medication - Comments
    Item
    Return of Study Medication - Comments
    text
    C2826299 (UMLS CUI [1,1])
    C0947611 (UMLS CUI [1,2])
    Back to the top of the page 

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