0 Ratings
ID

33572

Description

Study ID: 106904 Clinical Study ID: CRV106904 Study Title: A Randomized, Open-Label, Single-Dose, Four-Period Cross-Over Study to Determine the Effects of Alcohol on the Pharmacokinetics of Carvedilol CR 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: carvedilol Trade Name: Coreg CR,Coreg Study Indication: Hypertension

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Versions (2)
  1. 11/8/18 11/8/18 -
  2. 12/13/18 12/13/18 -
Copyright Holder

GSK group of companies

Uploaded on

December 13, 2018

DOI

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License

Creative Commons BY-NC 3.0
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    A Cross-Over Study of Alcohol Effect on the Pharmacokinetics of Carvedilol - 106904

    English

    Eligibility Question

    1 forms  
    1. StudyEvent: ODM
      1. Eligibility Question
    Administrative data
    Description

    Administrative data

    Alias
    UMLS CUI-1
    C1320722
    Site
    Description

    Site

    Data type

    text

    Alias
    UMLS CUI [1]
    C2825164
    Patient
    Description

    Patient

    Data type

    text

    Alias
    UMLS CUI [1]
    C1299487
    Patient Number
    Description

    Patient Number

    Data type

    integer

    Alias
    UMLS CUI [1,1]
    C0030705
    UMLS CUI [1,2]
    C1300638
    Eligibility Question
    Description

    Eligibility Question

    Alias
    UMLS CUI-1
    C1516637
    Did the subject meet all the entry criteria?
    Description

    Did the subject meet all the entry criteria?

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C1516637
    Do not admit he subject into this study if any Inclusion/Exclusion criteria is violated unless an exception has been granted by the GSK Medical Monitor and subject is continuing in the study. Please clarify the exemption(s) below
    Description

    Do not admit he subject into this study if any Inclusion/Exclusion criteria is violated unless an exception has been granted by the GSK Medical Monitor and subject is continuing in the study. Please clarify the exemption(s) below

    Data type

    text

    Alias
    UMLS CUI [1]
    C0030673
    UMLS CUI [2,1]
    C1512693
    UMLS CUI [2,2]
    C1709750
    UMLS CUI [3]
    C0680251
    Back to the top of the page

    Similar models

    Eligibility Question

    1 forms
    1. StudyEvent: ODM
      1. Eligibility Question
    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    Administrative data
    C1320722 (UMLS CUI-1)
    Site
    Item
    Site
    text
    C2825164 (UMLS CUI [1])
    Patient
    Item
    Patient
    text
    C1299487 (UMLS CUI [1])
    Patient Number
    Item
    Patient Number
    integer
    C0030705 (UMLS CUI [1,1])
    C1300638 (UMLS CUI [1,2])
    Item Group
    Eligibility Question
    C1516637 (UMLS CUI-1)
    Did the subject meet all the entry criteria?
    Item
    Did the subject meet all the entry criteria?
    boolean
    C1516637 (UMLS CUI [1])
    Do not admit he subject into this study if any Inclusion/Exclusion criteria is violated unless an exception has been granted by the GSK Medical Monitor and subject is continuing in the study. Please clarify the exemption(s) below
    Item
    Do not admit he subject into this study if any Inclusion/Exclusion criteria is violated unless an exception has been granted by the GSK Medical Monitor and subject is continuing in the study. Please clarify the exemption(s) below
    text
    C0030673 (UMLS CUI [1])
    C1512693 (UMLS CUI [2,1])
    C1709750 (UMLS CUI [2,2])
    C0680251 (UMLS CUI [3])
    Back to the top of the page 

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