0 Ratings

ID

32502

Description

Study ID: 106837 Clinical Study ID: HZA106837 Study Title: A Long-Term, Randomized, Double-Blind, Parallel Group Study of Fluticasone Furoate/GW642444 Inhalation Powder Once-Daily and Fluticasone Furoate Inhalation Powder Once-Daily in Subjects with Asthma Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT01086384 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 3 Study Recruitment Status: Completed Generic Name: fluticasone furoate/vilanterol Trade Name: Relvar Study Indication: Asthma

Keywords

  1. 11/5/18 11/5/18 -
  2. 12/4/18 12/4/18 -
Copyright Holder

GSK group of companies

Uploaded on

November 5, 2018

DOI

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License

Creative Commons BY-NC 3.0

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    A Parallel Group Study of Fluticasone Furoate/Vilanterol in Subjects with Asthma - 106837

    Pharmacogenetic Research Consent

    Pharmacogenetic (PGx) Research Consent/ Sample Collection
    Description

    Pharmacogenetic (PGx) Research Consent/ Sample Collection

    Has informed consent been obtained for PGx reearch?
    Description

    Has informed consent been obtained for PGx reearch?

    Data type

    boolean

    if YES, record date informed consent obtained for PGx research
    Description

    if YES, record date informed consent obtained for PGx research

    Data type

    text

    If NO, check reason
    Description

    If NO, check reason

    Data type

    text

    If OTHER, specify
    Description

    If OTHER, specify

    Data type

    text

    Has sample been collected for PGx research?
    Description

    Has sample been collected for PGx research?

    Data type

    boolean

    If YES, record the date sample taken
    Description

    If YES, record the date sample taken

    Data type

    date

    Sample Type
    Description

    Sample Type

    Record Sample Type
    Description

    Record Sample Type

    Data type

    text

    Similar models

    Pharmacogenetic Research Consent

    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    Pharmacogenetic (PGx) Research Consent/ Sample Collection
    Has informed consent been obtained for PGx reearch?
    Item
    Has informed consent been obtained for PGx reearch?
    boolean
    if YES, record date informed consent obtained for PGx research
    Item
    if YES, record date informed consent obtained for PGx research
    text
    Item
    If NO, check reason
    text
    Code List
    If NO, check reason
    CL Item
    [1] Subject declined (1)
    CL Item
    [2] Subject not asked by Investigator (2)
    CL Item
    [Z] Other (3)
    If OTHER, specify
    Item
    If OTHER, specify
    text
    Has sample been collected for PGx research?
    Item
    Has sample been collected for PGx research?
    boolean
    If YES, record the date sample taken
    Item
    If YES, record the date sample taken
    date
    Item Group
    Sample Type
    Record Sample Type
    Item
    Record Sample Type
    text

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