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ID

39231

Description

Study ID: 111569 Clinical Study ID: 111569 Study Title: A fixed dose, dose-response study for ropinirole prolonged release (PR) as adjunctive treatment to L-Dopa in patients with advanced Parkinson's disease Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT01494532 Sponsor: GlaxoSmithKline Phase: Phase 4 Study Recruitment Status: Completed Generic Name: Ropinirole, placebo Study Indication: Parkinson's Disease

Keywords

Versions (7)
  1. 12/11/19 12/11/19 -
  2. 12/11/19 12/11/19 -
  3. 12/11/19 12/11/19 -
  4. 12/11/19 12/11/19 -
  5. 12/16/19 12/16/19 -
  6. 1/9/20 1/9/20 -
  7. 1/9/20 1/9/20 -
Copyright Holder

GlaxoSmithKline

Uploaded on

December 11, 2019

DOI

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License

Creative Commons BY-NC 3.0
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    Ropinirole prolonged release (PR) as adjunctive treatment to L-Dopa in patients with advanced Parkinson's disease

    English

    Visit 4; Visit 6: Visit 8 - Pregnancy

    1 forms  
    Administration
    Description

    Administration

    Alias
    UMLS CUI-1
    C1320722
    Study Name
    Description

    Study Name

    Data type

    text

    Alias
    UMLS CUI [1]
    C2348560
    Subject ID
    Description

    Subject ID

    Data type

    text

    Alias
    UMLS CUI [1]
    C2348585
    Study Site
    Description

    Study Site

    Data type

    text

    Alias
    UMLS CUI [1]
    C2825164
    Pregnancy
    Description

    Pregnancy

    Alias
    UMLS CUI-1
    C0032961
    Did a female partner of a male subject become pregnant during the study?
    Description

    Did a female partner of a male subject become pregnant during the study?

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0919624
    Did the subject become pregnant during the study?
    Description

    Did the subject become pregnant during the study?

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0032961
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    Similar models

    Visit 4; Visit 6: Visit 8 - Pregnancy

    1 forms
    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    Administration
    C1320722 (UMLS CUI-1)
    Study Name
    Item
    Study Name
    text
    C2348560 (UMLS CUI [1])
    Subject ID
    Item
    Subject ID
    text
    C2348585 (UMLS CUI [1])
    Study Site
    Item
    Study Site
    text
    C2825164 (UMLS CUI [1])
    Item Group
    Pregnancy
    C0032961 (UMLS CUI-1)
    Did a female partner of a male subject become pregnant during the study?
    Item
    Did a female partner of a male subject become pregnant during the study?
    boolean
    C0919624 (UMLS CUI [1])
    Did the subject become pregnant during the study?
    Item
    Did the subject become pregnant during the study?
    boolean
    C0032961 (UMLS CUI [1])
    Back to the top of the page 

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