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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

Mots-clés

  1. 09/10/2017 09/10/2017 -
Détendeur de droits

GlaxoSmithKline

Téléchargé le

9 octobre 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0

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

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

    Form D
    Description

    Form D

    Alias
    UMLS CUI-1
    C0011065
    Certified Cause of Death
    Description

    Certified Cause of Death

    Type de données

    text

    Alias
    UMLS CUI [1]
    C0007465
    Date of Death
    Description

    Date of Death

    Type de données

    date

    Alias
    UMLS CUI [1,1]
    C0011065
    UMLS CUI [1,2]
    C0011008
    Was a post-mortem carried out?
    Description

    post-mortem

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0004398
    If Yes, please summarize findings (include diagnosis):
    Description

    Was a post-mortem carried out?

    Type de données

    text

    Alias
    UMLS CUI [1]
    C0004398

    Similar models

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

    Name
    Type
    Description | Question | Decode (Coded Value)
    Type de données
    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])

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