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ID

33300

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

Mots-clés

Versions (2)
  1. 05/11/2018 05/11/2018 -
  2. 04/12/2018 04/12/2018 -
Détendeur de droits

GSK group of companies

Téléchargé le

4 décembre 2018

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0
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    A Parallel Group Study of Fluticasone Furoate/Vilanterol in Subjects with Asthma - 106837

    Anglais

    Pharmacogenetic Research Consent

    1 Formulaires  
    Pharmacogenetic (PGx) Research Consent/ Sample Collection
    Description

    Pharmacogenetic (PGx) Research Consent/ Sample Collection

    Alias
    UMLS CUI-1
    C0031325
    UMLS CUI-2
    C0035168
    UMLS CUI-3
    C1511481
    UMLS CUI-4
    C0200345
    Has informed consent been obtained for PGx research?
    Description

    Has informed consent been obtained for PGx reearch?

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0021430
    UMLS CUI [2,1]
    C0031325
    UMLS CUI [2,2]
    C0035168
    if YES, record date informed consent obtained for PGx research
    Description

    if YES, record date informed consent obtained for PGx research

    Type de données

    text

    Alias
    UMLS CUI [1]
    C2985782
    UMLS CUI [2,1]
    C0031325
    UMLS CUI [2,2]
    C0035168
    If NO, check reason for informed consent not being obtained.
    Description

    If NO, check reason

    Type de données

    text

    Alias
    UMLS CUI [1,1]
    C0021430
    UMLS CUI [1,2]
    C1882120
    UMLS CUI [1,3]
    C0392360
    If OTHER, specify
    Description

    If OTHER, specify

    Type de données

    text

    Alias
    UMLS CUI [1,1]
    C0021430
    UMLS CUI [1,2]
    C1882120
    UMLS CUI [1,3]
    C0392360
    UMLS CUI [1,4]
    C0205394
    UMLS CUI [1,5]
    C2348235
    Has sample been collected for PGx research?
    Description

    Has sample been collected for PGx research?

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0200345
    UMLS CUI [2,1]
    C0031325
    UMLS CUI [2,2]
    C0035168
    If YES, record the date sample taken
    Description

    If YES, record the date sample taken

    Type de données

    date

    Alias
    UMLS CUI [1]
    C1302413
    Sample Type
    Description

    Sample Type

    Alias
    UMLS CUI-1
    C2347029
    Record Sample Type
    Description

    Record Sample Type

    Type de données

    text

    Alias
    UMLS CUI [1]
    C2347029
    Retour au début de la page

    Similar models

    Pharmacogenetic Research Consent

    1 Formulaires
    Name
    Type
    Description | Question | Decode (Coded Value)
    Type de données
    Alias
    Item Group
    Pharmacogenetic (PGx) Research Consent/ Sample Collection
    C0031325 (UMLS CUI-1)
    C0035168 (UMLS CUI-2)
    C1511481 (UMLS CUI-3)
    C0200345 (UMLS CUI-4)
    Has informed consent been obtained for PGx reearch?
    Item
    Has informed consent been obtained for PGx research?
    boolean
    C0021430 (UMLS CUI [1])
    C0031325 (UMLS CUI [2,1])
    C0035168 (UMLS CUI [2,2])
    if YES, record date informed consent obtained for PGx research
    Item
    if YES, record date informed consent obtained for PGx research
    text
    C2985782 (UMLS CUI [1])
    C0031325 (UMLS CUI [2,1])
    C0035168 (UMLS CUI [2,2])
    Item
    If NO, check reason for informed consent not being obtained.
    text
    C0021430 (UMLS CUI [1,1])
    C1882120 (UMLS CUI [1,2])
    C0392360 (UMLS CUI [1,3])
    If NO, check reason
    Code List
    If NO, check reason for informed consent not being obtained.
    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
    C0021430 (UMLS CUI [1,1])
    C1882120 (UMLS CUI [1,2])
    C0392360 (UMLS CUI [1,3])
    C0205394 (UMLS CUI [1,4])
    C2348235 (UMLS CUI [1,5])
    Has sample been collected for PGx research?
    Item
    Has sample been collected for PGx research?
    boolean
    C0200345 (UMLS CUI [1])
    C0031325 (UMLS CUI [2,1])
    C0035168 (UMLS CUI [2,2])
    If YES, record the date sample taken
    Item
    If YES, record the date sample taken
    date
    C1302413 (UMLS CUI [1])
    Item Group
    Sample Type
    C2347029 (UMLS CUI-1)
    Record Sample Type
    Item
    Record Sample Type
    text
    C2347029 (UMLS CUI [1])
    Retour au début de la page 

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