ID

26452

Beschrijving

Study ID: 101468/168 Clinical Study ID: 101468/168 Study Title: A Randomised, Double Blind, Three Period, Cross-Over Study of Ropinirole CR and Ropinirole IR Monotherapy Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 3 Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: Modutab,ZIPEREVE,ZEPREVE,REPREVE,ADARTREL,REQUIP,Zygara Study Indication: Parkinson Disease

Trefwoorden

Versies (1)
  1. 17-10-17 17-10-17 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

17 oktober 2017

DOI

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Licentie

Creative Commons BY-NC 3.0
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    Unscheduled visit 3 compliance Ropinirole CR Ropinirole IR Monotherapy 101468/168

    Engels

    Unscheduled visit 3 compliance Ropinirole CR Ropinirole IR Monotherapy 101468/168

    1 Formulieren  
    Administrative Data
    Beschrijving

    Administrative Data

    Alias
    UMLS CUI-1
    C1320722
    Subject Number
    Beschrijving

    subject number

    Datatype

    integer

    Alias
    UMLS CUI [1]
    C2348585
    RANDOMISATION NUMBER
    Beschrijving

    randomisation number

    Datatype

    integer

    Alias
    UMLS CUI [1,1]
    C0034656
    UMLS CUI [1,2]
    C0237753
    INVESTIGATIONAL PRODUCT
    Beschrijving

    INVESTIGATIONAL PRODUCT

    Alias
    UMLS CUI-1
    C0304229
    Investigational Product
    Beschrijving

    investigational product

    Datatype

    text

    Alias
    UMLS CUI [1]
    C0304229
    Blinded Dose Level
    Beschrijving

    medication dosage

    Datatype

    integer

    Alias
    UMLS CUI [1,1]
    C0178602
    UMLS CUI [1,2]
    C0304229
    Start Date
    Beschrijving

    start date

    Datatype

    date

    Alias
    UMLS CUI [1]
    C0808070
    Stop Date
    Beschrijving

    stop date

    Datatype

    date

    Alias
    UMLS CUI [1]
    C0806020
    Investigational product Container Number
    Beschrijving

    investigational product container number

    Datatype

    integer

    Alias
    UMLS CUI [1,1]
    C3898691
    UMLS CUI [1,2]
    C0449788
    COMPLIANCE
    Beschrijving

    COMPLIANCE

    Alias
    UMLS CUI-1
    C1321605
    Total Number of Tablets Dispensed
    Beschrijving

    total number of tablets dispensed

    Datatype

    integer

    Alias
    UMLS CUI [1,1]
    C0805077
    UMLS CUI [1,2]
    C0039225
    Total Number of Tablets Returned
    Beschrijving

    total number of tablets returned

    Datatype

    integer

    Alias
    UMLS CUI [1,1]
    C2699071
    UMLS CUI [1,2]
    C0039225
    Has the subject missed investigational product for > 3 consecutive days?
    Beschrijving

    investigational product compliance

    Datatype

    text

    Alias
    UMLS CUI [1,1]
    C0304229
    UMLS CUI [1,2]
    C1321605
    Terug naar het begin van de pagina

    Similar models

    Unscheduled visit 3 compliance Ropinirole CR Ropinirole IR Monotherapy 101468/168

    1 Formulieren
    Name
    Type
    Description | Question | Decode (Coded Value)
    Datatype
    Alias
    Item Group
    Administrative Data
    C1320722 (UMLS CUI-1)
    subject number
    Item
    Subject Number
    integer
    C2348585 (UMLS CUI [1])
    randomisation number
    Item
    RANDOMISATION NUMBER
    integer
    C0034656 (UMLS CUI [1,1])
    C0237753 (UMLS CUI [1,2])
    Item Group
    INVESTIGATIONAL PRODUCT
    C0304229 (UMLS CUI-1)
    Item
    Investigational Product
    text
    C0304229 (UMLS CUI [1])
    investigational product
    Code List
    Investigational Product
    CL Item
    Bottle A (Bottle A)
    CL Item
    Bottle B (Bottle B)
    medication dosage
    Item
    Blinded Dose Level
    integer
    C0178602 (UMLS CUI [1,1])
    C0304229 (UMLS CUI [1,2])
    start date
    Item
    Start Date
    date
    C0808070 (UMLS CUI [1])
    stop date
    Item
    Stop Date
    date
    C0806020 (UMLS CUI [1])
    investigational product container number
    Item
    Investigational product Container Number
    integer
    C3898691 (UMLS CUI [1,1])
    C0449788 (UMLS CUI [1,2])
    Item Group
    COMPLIANCE
    C1321605 (UMLS CUI-1)
    total number of tablets dispensed
    Item
    Total Number of Tablets Dispensed
    integer
    C0805077 (UMLS CUI [1,1])
    C0039225 (UMLS CUI [1,2])
    total number of tablets returned
    Item
    Total Number of Tablets Returned
    integer
    C2699071 (UMLS CUI [1,1])
    C0039225 (UMLS CUI [1,2])
    Item
    Has the subject missed investigational product for > 3 consecutive days?
    text
    C0304229 (UMLS CUI [1,1])
    C1321605 (UMLS CUI [1,2])
    investigational product compliance
    Code List
    Has the subject missed investigational product for > 3 consecutive days?
    CL Item
    Yes (Y)
    CL Item
    No (N)
    Terug naar het begin van de pagina 

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