0 Ratings
ID

26113

Description

Study ID: 101468/219 Clinical Study ID: 101468/219 Study Title:An open label, randomised, five-way crossover single-dose pharmacokinetic study to assess dosage strength equivalence of ropinirole CR in healthy male and female volunteers Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 1 Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: Requip Study Indication : Parkinson Disease Documentation part: Form D

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Versions (1)
  1. 10/9/17 10/9/17 -
Copyright Holder

GlaxoSmithKline

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October 9, 2017

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Creative Commons BY-NC 3.0
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    Dose strength equivalence of ropinirole CR in healthy adults Form D 101468/219

    English

    Form D Dose strength equivalence of ropinirole CR in healthy adults 101468/219

    1 forms  
    Form D
    Description

    Form D

    Alias
    UMLS CUI-1
    C0011065 (Cessation of life)
    SNOMED
    419620001
    Certified Cause of Death
    Description

    Certified Cause of Death

    Data type

    text

    Alias
    UMLS CUI [1]
    C0007465 (Cause of Death)
    SNOMED
    16100001
    LOINC
    LA10595-9
    Date of Death
    Description

    Date of Death

    Data type

    date

    Alias
    UMLS CUI [1,1]
    C0011065 (Cessation of life)
    SNOMED
    419620001
    UMLS CUI [1,2]
    C0011008 (Date in time)
    SNOMED
    410671006
    Was a post-mortem carried out?
    Description

    post-mortem

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0004398 (Autopsy)
    SNOMED
    29240004
    LOINC
    LA20097-4
    If Yes, please summarize findings (include diagnosis):
    Description

    Was a post-mortem carried out?

    Data type

    text

    Alias
    UMLS CUI [1]
    C0004398 (Autopsy)
    SNOMED
    29240004
    LOINC
    LA20097-4
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    Similar models

    Form D Dose strength equivalence of ropinirole CR in healthy adults 101468/219

    1 forms
    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    Form D
    C0011065 (UMLS CUI-1)
    Certified Cause of Death
    Item
    Certified Cause of Death
    text
    C0007465 (UMLS CUI [1])
    Date of Death
    Item
    Date of Death
    date
    C0011065 (UMLS CUI [1,1])
    C0011008 (UMLS CUI [1,2])
    post-mortem
    Item
    Was a post-mortem carried out?
    boolean
    C0004398 (UMLS CUI [1])
    post-mortem
    Item
    If Yes, please summarize findings (include diagnosis):
    text
    C0004398 (UMLS CUI [1])
    Back to the top of the page 

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