0 Evaluaciones
ID

26109

Descripción

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: Concomitant Medication

Palabras clave

Versiones (1)
  1. 09/10/17 09/10/17 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

9 ottobre 2017

DOI

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Licencia

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

    Inglés

    Concomitant Medication Dose strength equivalence of ropinirole CR in healthy adults 101468/219

    1 formularios  
    Concomitant Medication
    Descripción

    Concomitant Medication

    Alias
    UMLS CUI-1
    C2347852
    UMLS CUI-2
    C0244821
    Are there any concomitant medication CHANGES since the start of the study?
    Descripción

    If ’YES’, please record all medications used below. Where appropriate, medical conditions should be recorded on the Adverse Events Form, utilizing the same terminology. If a medication has had a dosage change it must be recorded with the start and stop date.

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C2347852
    drug name
    Descripción

    Trade Name Preferred

    Tipo de datos

    text

    Alias
    UMLS CUI [1,1]
    C2360065
    UMLS CUI [1,2]
    C2347852
    Single Dose/Unit
    Descripción

    dose per unit

    Tipo de datos

    integer

    Alias
    UMLS CUI [1,1]
    C3174092
    UMLS CUI [1,2]
    C2347852
    Frequency of this Dose
    Descripción

    medication frequency

    Tipo de datos

    text

    Alias
    UMLS CUI [1,1]
    C3476109
    UMLS CUI [1,2]
    C2347852
    Route
    Descripción

    drug application route

    Tipo de datos

    text

    Alias
    UMLS CUI [1,1]
    C0013153
    UMLS CUI [1,2]
    C2347852
    Indication
    Descripción

    medication indication

    Tipo de datos

    text

    Alias
    UMLS CUI [1,1]
    C3146298
    UMLS CUI [1,2]
    C2347852
    Duration
    Descripción

    duration of medication

    Tipo de datos

    text

    Alias
    UMLS CUI [1,1]
    C0449238
    UMLS CUI [1,2]
    C2347852
    End Date
    Descripción

    end date of medication

    Tipo de datos

    date

    Alias
    UMLS CUI [1,1]
    C2347852
    UMLS CUI [1,2]
    C0806020
    Continuing at end of study?
    Descripción

    continuing medication

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C2826666
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    Similar models

    Concomitant Medication Dose strength equivalence of ropinirole CR in healthy adults 101468/219

    1 formularios
    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de datos
    Alias
    Item Group
    Concomitant Medication
    C2347852 (UMLS CUI-1)
    C0244821 (UMLS CUI-2)
    concomitant medication
    Item
    Are there any concomitant medication CHANGES since the start of the study?
    boolean
    C2347852 (UMLS CUI [1])
    drug name
    Item
    drug name
    text
    C2360065 (UMLS CUI [1,1])
    C2347852 (UMLS CUI [1,2])
    dose per unit
    Item
    Single Dose/Unit
    integer
    C3174092 (UMLS CUI [1,1])
    C2347852 (UMLS CUI [1,2])
    medication frequency
    Item
    Frequency of this Dose
    text
    C3476109 (UMLS CUI [1,1])
    C2347852 (UMLS CUI [1,2])
    drug application route
    Item
    Route
    text
    C0013153 (UMLS CUI [1,1])
    C2347852 (UMLS CUI [1,2])
    medication indication
    Item
    Indication
    text
    C3146298 (UMLS CUI [1,1])
    C2347852 (UMLS CUI [1,2])
    duration of medication
    Item
    Duration
    text
    C0449238 (UMLS CUI [1,1])
    C2347852 (UMLS CUI [1,2])
    end date of medication
    Item
    End Date
    date
    C2347852 (UMLS CUI [1,1])
    C0806020 (UMLS CUI [1,2])
    continuing medication
    Item
    Continuing at end of study?
    boolean
    C2826666 (UMLS CUI [1])
    Volver a la parte superior de la página 

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