ID

23002

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

Keywords

  1. 6/19/17 6/19/17 -
Uploaded on

June 19, 2017

DOI

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License

Creative Commons BY-NC 3.0

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    Status of Treatment Blind - GSK Milveterol COPD 100527

    Status of Treatment Blind - GSK Milveterol COPD 100527

    Status of Treatment Blind
    Description

    Status of Treatment Blind

    Alias
    UMLS CUI-1
    C2347038
    UMLS CUI-2
    C0449438
    Was the treatment blind for this subject broken during the study?
    Description

    blind broken

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C3897431
    UMLS CUI [1,2]
    C2347038
    lf 'Yes', date of subject unblinding:
    Description

    Date of subject unblinding

    Data type

    date

    Measurement units
    • dd.mm.yyyy
    Alias
    UMLS CUI [1,1]
    C0011008
    UMLS CUI [1,2]
    C3897431
    dd.mm.yyyy
    If 'Yes', reason for subject unblinding:
    Description

    Reason for subject unblinding

    Data type

    integer

    Alias
    UMLS CUI [1,1]
    C0566251
    UMLS CUI [1,2]
    C3897431
    If 'Other', please specify:
    Description

    Specification reason for unblinding

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C2348235
    UMLS CUI [1,2]
    C0566251
    UMLS CUI [1,3]
    C3897431

    Similar models

    Status of Treatment Blind - GSK Milveterol COPD 100527

    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    Status of Treatment Blind
    C2347038 (UMLS CUI-1)
    C0449438 (UMLS CUI-2)
    blind broken
    Item
    Was the treatment blind for this subject broken during the study?
    boolean
    C3897431 (UMLS CUI [1,1])
    C2347038 (UMLS CUI [1,2])
    Date of subject unblinding
    Item
    lf 'Yes', date of subject unblinding:
    date
    C0011008 (UMLS CUI [1,1])
    C3897431 (UMLS CUI [1,2])
    Item
    If 'Yes', reason for subject unblinding:
    integer
    C0566251 (UMLS CUI [1,1])
    C3897431 (UMLS CUI [1,2])
    Code List
    If 'Yes', reason for subject unblinding:
    CL Item
    Medical emergency requiring identity of investigational product for further treatment (1)
    CL Item
    Other (please specify below) (2)
    Specification reason for unblinding
    Item
    If 'Other', please specify:
    text
    C2348235 (UMLS CUI [1,1])
    C0566251 (UMLS CUI [1,2])
    C3897431 (UMLS CUI [1,3])

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