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ID

33370

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

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Versions (2)
  1. 06/11/2018 06/11/2018 -
  2. 06/12/2018 06/12/2018 -
Détendeur de droits

GSK group of companies

Téléchargé le

6 décembre 2018

DOI

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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

    Pharmacogenetik Research Consent Withdrawal

    1 Formulaires  
    Withdrawal of concent for PGx/Sample Destruction
    Description

    Withdrawal of concent for PGx/Sample Destruction

    Alias
    UMLS CUI-1
    C0031325 (Pharmacogenetics)
    UMLS CUI-2
    C0035168 (research)
    UMLS CUI-3
    C1707492 (Consent Withdrawn)
    UMLS CUI-4
    C1948029 (Destruction (action))
    UMLS CUI-5
    C0178913 (Blood specimen)
    SNOMED
    119297000
    Has subject withdrawn consent for PGx research?
    Description

    Has subject withdrawn consent for PGx research?

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C0031325 (Pharmacogenetics)
    UMLS CUI [1,2]
    C0035168 (research)
    UMLS CUI [1,3]
    C1707492 (Consent Withdrawn)
    If YES, record the date consent withdrawn
    Description

    If YES, record the date consent withdrawn

    Type de données

    date

    Alias
    UMLS CUI [1,1]
    C0031325 (Pharmacogenetics)
    UMLS CUI [1,2]
    C0035168 (research)
    UMLS CUI [1,3]
    C1707492 (Consent Withdrawn)
    UMLS CUI [1,4]
    C0011008 (Date in time)
    SNOMED
    410671006
    Has a request been made for sample destruction?
    Description

    Has a request been made for sample destruction?

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C1948029 (Destruction (action))
    UMLS CUI [1,2]
    C0178913 (Blood specimen)
    SNOMED
    119297000
    UMLS CUI [1,3]
    C1272683 (Request - action)
    SNOMED
    385644000
    If YES, check reason
    Description

    If YES, check reason

    Type de données

    text

    Alias
    UMLS CUI [1,1]
    C1948029 (Destruction (action))
    UMLS CUI [1,2]
    C0178913 (Blood specimen)
    SNOMED
    119297000
    UMLS CUI [1,3]
    C1272683 (Request - action)
    SNOMED
    385644000
    UMLS CUI [1,4]
    C0392360 (Indication of (contextual qualifier))
    SNOMED
    230165009
    LOINC
    MTHU008319
    If OTHER, specify
    Description

    If OTHER, specify

    Type de données

    text

    Alias
    UMLS CUI [1,1]
    C1948029 (Destruction (action))
    UMLS CUI [1,2]
    C0178913 (Blood specimen)
    SNOMED
    119297000
    UMLS CUI [1,3]
    C1272683 (Request - action)
    SNOMED
    385644000
    UMLS CUI [1,4]
    C0392360 (Indication of (contextual qualifier))
    SNOMED
    230165009
    LOINC
    MTHU008319
    UMLS CUI [2,1]
    C0205394 (Other)
    SNOMED
    74964007
    LOINC
    LP21049-9
    UMLS CUI [2,2]
    C2348235 (Specification)
    Sample type
    Description

    Sample type

    Type de données

    text

    Alias
    UMLS CUI [1]
    C2347029 (Biospecimen Type)
    Retour au début de la page

    Similar models

    Pharmacogenetik Research Consent Withdrawal

    1 Formulaires
    Name
    Type
    Description | Question | Decode (Coded Value)
    Type de données
    Alias
    Item Group
    Withdrawal of concent for PGx/Sample Destruction
    C0031325 (UMLS CUI-1)
    C0035168 (UMLS CUI-2)
    C1707492 (UMLS CUI-3)
    C1948029 (UMLS CUI-4)
    C0178913 (UMLS CUI-5)
    Has subject withdrawn consent for PGx research?
    Item
    Has subject withdrawn consent for PGx research?
    boolean
    C0031325 (UMLS CUI [1,1])
    C0035168 (UMLS CUI [1,2])
    C1707492 (UMLS CUI [1,3])
    If YES, record the date consent withdrawn
    Item
    If YES, record the date consent withdrawn
    date
    C0031325 (UMLS CUI [1,1])
    C0035168 (UMLS CUI [1,2])
    C1707492 (UMLS CUI [1,3])
    C0011008 (UMLS CUI [1,4])
    Has a request been made for sample destruction?
    Item
    Has a request been made for sample destruction?
    boolean
    C1948029 (UMLS CUI [1,1])
    C0178913 (UMLS CUI [1,2])
    C1272683 (UMLS CUI [1,3])
    Item
    If YES, check reason
    text
    C1948029 (UMLS CUI [1,1])
    C0178913 (UMLS CUI [1,2])
    C1272683 (UMLS CUI [1,3])
    C0392360 (UMLS CUI [1,4])
    If YES, check reason
    Code List
    If YES, check reason
    CL Item
    Subject withdrew consent for PGx (1)
    CL Item
    Screen failure (2)
    CL Item
    Other (3)
    If OTHER, specify
    Item
    If OTHER, specify
    text
    C1948029 (UMLS CUI [1,1])
    C0178913 (UMLS CUI [1,2])
    C1272683 (UMLS CUI [1,3])
    C0392360 (UMLS CUI [1,4])
    C0205394 (UMLS CUI [2,1])
    C2348235 (UMLS CUI [2,2])
    Sample type
    Item
    Sample type
    text
    C2347029 (UMLS CUI [1])
    Retour au début de la page 

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