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ID

33370

Beschreibung

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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Versionen (2)
  1. 06.11.18 06.11.18 -
  2. 06.12.18 06.12.18 -
Rechteinhaber

GSK group of companies

Hochgeladen am

6. Dezember 2018

DOI

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

    Englisch

    Pharmacogenetik Research Consent Withdrawal

    1 Formulare  
    Withdrawal of concent for PGx/Sample Destruction
    Beschreibung

    Withdrawal of concent for PGx/Sample Destruction

    Alias
    UMLS CUI-1
    C0031325
    UMLS CUI-2
    C0035168
    UMLS CUI-3
    C1707492
    UMLS CUI-4
    C1948029
    UMLS CUI-5
    C0178913
    Has subject withdrawn consent for PGx research?
    Beschreibung

    Has subject withdrawn consent for PGx research?

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0031325
    UMLS CUI [1,2]
    C0035168
    UMLS CUI [1,3]
    C1707492
    If YES, record the date consent withdrawn
    Beschreibung

    If YES, record the date consent withdrawn

    Datentyp

    date

    Alias
    UMLS CUI [1,1]
    C0031325
    UMLS CUI [1,2]
    C0035168
    UMLS CUI [1,3]
    C1707492
    UMLS CUI [1,4]
    C0011008
    Has a request been made for sample destruction?
    Beschreibung

    Has a request been made for sample destruction?

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C1948029
    UMLS CUI [1,2]
    C0178913
    UMLS CUI [1,3]
    C1272683
    If YES, check reason
    Beschreibung

    If YES, check reason

    Datentyp

    text

    Alias
    UMLS CUI [1,1]
    C1948029
    UMLS CUI [1,2]
    C0178913
    UMLS CUI [1,3]
    C1272683
    UMLS CUI [1,4]
    C0392360
    If OTHER, specify
    Beschreibung

    If OTHER, specify

    Datentyp

    text

    Alias
    UMLS CUI [1,1]
    C1948029
    UMLS CUI [1,2]
    C0178913
    UMLS CUI [1,3]
    C1272683
    UMLS CUI [1,4]
    C0392360
    UMLS CUI [2,1]
    C0205394
    UMLS CUI [2,2]
    C2348235
    Sample type
    Beschreibung

    Sample type

    Datentyp

    text

    Alias
    UMLS CUI [1]
    C2347029
    Zum Seitenanfang zurückkehren

    Ähnliche Modelle

    Pharmacogenetik Research Consent Withdrawal

    1 Formulare
    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datentyp
    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])
    Zum Seitenanfang zurückkehren 

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