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23007

Description

Study ID: 100527 Clinical Study ID: B2E100527 Study Title: A randomised, double blind, placebo controlled, parellel group study to examine the efficacy, safety, tolerability and systemic pharmacokinetic profile of repeated inhaled doses of GSK159797 Sponsor: GlaxoSmithKline Phase: phase 2 Study Recruitment Status: Completed Generic Name: milveterol Trade Name: Milveterol Study Indication: Pulmonary Disease, Chronic Obstructive

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  1. 19/06/2017 19/06/2017 -
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19 juin 2017

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Creative Commons BY-NC 3.0
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    End of Study Record - GSK Milveterol COPD 100527

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    End of Study Record - GSK Milveterol COPD 100527

    1 Formulaires  
    End of Study Record
    Description

    End of Study Record

    Alias
    UMLS CUI-1
    C0008976
    UMLS CUI-2
    C0444930
    Date of subject completion or discontinuation from the study
    Description

    Date of subject completion or discontinuation from the study

    Type de données

    date

    Unités de mesure
    • dd.mm.yyyy
    Alias
    UMLS CUI [1,1]
    C2348577
    UMLS CUI [1,2]
    C0011008
    dd.mm.yyyy
    Time of subject completion or discontinuation from the study
    Description

    Time of subject completion or discontinuation from the study

    Type de données

    time

    Unités de mesure
    • hh:mm
    Alias
    UMLS CUI [1,1]
    C2348577
    UMLS CUI [1,2]
    C0040223
    hh:mm
    Did the subject discontinue the study prematurely?
    Description

    premature discontinuation of study

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C2348577
    UMLS CUI [1,2]
    C1279919
    If 'Yes', the primary reason for discontinuation:
    Description

    Reason for premature discontinuation

    Type de données

    integer

    Alias
    UMLS CUI [1,1]
    C0566251
    UMLS CUI [1,2]
    C2348577
    UMLS CUI [1,3]
    C1279919
    If 'Other', please specify:
    Description

    Specification reason for discontinuation

    Type de données

    text

    Alias
    UMLS CUI [1,1]
    C2348235
    UMLS CUI [1,2]
    C0566251
    UMLS CUI [1,3]
    C2348577
    UMLS CUI [1,4]
    C1279919
    Retour au début de la page

    Similar models

    End of Study Record - GSK Milveterol COPD 100527

    1 Formulaires
    Name
    Type
    Description | Question | Decode (Coded Value)
    Type de données
    Alias
    Item Group
    End of Study Record
    C0008976 (UMLS CUI-1)
    C0444930 (UMLS CUI-2)
    Date of subject completion or discontinuation from the study
    Item
    Date of subject completion or discontinuation from the study
    date
    C2348577 (UMLS CUI [1,1])
    C0011008 (UMLS CUI [1,2])
    Time of subject completion or discontinuation from the study
    Item
    Time of subject completion or discontinuation from the study
    time
    C2348577 (UMLS CUI [1,1])
    C0040223 (UMLS CUI [1,2])
    premature discontinuation of study
    Item
    Did the subject discontinue the study prematurely?
    boolean
    C2348577 (UMLS CUI [1,1])
    C1279919 (UMLS CUI [1,2])
    Item
    If 'Yes', the primary reason for discontinuation:
    integer
    C0566251 (UMLS CUI [1,1])
    C2348577 (UMLS CUI [1,2])
    C1279919 (UMLS CUI [1,3])
    Reason for premature discontinuation
    Code List
    If 'Yes', the primary reason for discontinuation:
    CL Item
    Adverse event (1)
    CL Item
    Consent withdrawn (2)
    CL Item
    Lost to follow up (3)
    CL Item
    Protocol violation (4)
    CL Item
    Other (please specify below) (5)
    Specification reason for discontinuation
    Item
    If 'Other', please specify:
    text
    C2348235 (UMLS CUI [1,1])
    C0566251 (UMLS CUI [1,2])
    C2348577 (UMLS CUI [1,3])
    C1279919 (UMLS CUI [1,4])
    Retour au début de la page 

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