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ID

32502

Descrizione

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. 05/11/18 05/11/18 -
  2. 04/12/18 04/12/18 -
Titolare del copyright

GSK group of companies

Caricato su

5 novembre 2018

DOI

Per favore, per richiedere un accesso.

Licenza

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
    Descrizione

    Pharmacogenetic (PGx) Research Consent/ Sample Collection

    Has informed consent been obtained for PGx reearch?
    Descrizione

    Has informed consent been obtained for PGx reearch?

    Tipo di dati

    boolean

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

    if YES, record date informed consent obtained for PGx research

    Tipo di dati

    text

    If NO, check reason
    Descrizione

    If NO, check reason

    Tipo di dati

    text

    If OTHER, specify
    Descrizione

    If OTHER, specify

    Tipo di dati

    text

    Has sample been collected for PGx research?
    Descrizione

    Has sample been collected for PGx research?

    Tipo di dati

    boolean

    If YES, record the date sample taken
    Descrizione

    If YES, record the date sample taken

    Tipo di dati

    date

    Sample Type
    Descrizione

    Sample Type

    Record Sample Type
    Descrizione

    Record Sample Type

    Tipo di dati

    text

    Similar models

    Pharmacogenetic Research Consent

    Name
    genere
    Description | Question | Decode (Coded Value)
    Tipo di dati
    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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