ID

28410

Descrizione

Study ID: 100601 Clinical Study ID: LPL100601 Study Title: LPL100601, A Clinical Outcomes Study of Darapladib versus Placebo in Subjects with Chronic Coronary Heart Disease to Compare the Incidence of Major Adverse Cardiovascular Events (MACE) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00799903 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 3 Study Recruitment Status: Completed Generic Name: darapladib Trade Name: darapladib Study Indication: Atherosclerosis Study part: Pharmacogenetic research Withdrawal of consent

Keywords

  1. 09/10/17 09/10/17 -
  2. 16/10/17 16/10/17 -
  3. 23/10/17 23/10/17 -
  4. 11/01/18 11/01/18 -
Titolare del copyright

GlaxoSmithKline

Caricato su

11 gennaio 2018

DOI

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Licenza

Creative Commons BY-NC 3.0

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    Pharmacogenetic research Withdrawal of consent GSK study Chronic Coronary Heart Disease NCT00799903

    Pharmacogenetic research Withdrawal of consent Subject Identification GSK study Chronic Coronary Heart Disease NCT00799903

    Withdrawal of consent for PGx (DNA) / Blood sample destruction
    Descrizione

    Withdrawal of consent for PGx (DNA) / Blood sample destruction

    1. Has subject withdrawn consent for PGx research?
    Descrizione

    withdrawal consent for PGx research

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1,1]
    C0021430
    UMLS CUI [1,2]
    C2347500
    If subject has withdrawn consent for PGx research: date informed consent withdrawn
    Descrizione

    date informed consent withdrawn

    Tipo di dati

    date

    Alias
    UMLS CUI [1]
    C2985782
    2. Has a request been made for blood sample destruction?
    Descrizione

    request for blood sample destruction

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1,1]
    C1948029
    UMLS CUI [1,2]
    C0178913
    UMLS CUI [1,3]
    C1272683
    If a request has been made for blood sample destruction, check reason
    Descrizione

    request for blood sample destruction reason

    Tipo di dati

    text

    Alias
    UMLS CUI [1,1]
    C1948029
    UMLS CUI [1,2]
    C0178913
    UMLS CUI [1,3]
    C0392360
    If other reason applied, specify
    Descrizione

    request for blood sample destruction other reason

    Tipo di dati

    text

    Alias
    UMLS CUI [1,1]
    C0566251
    UMLS CUI [1,2]
    C1272683
    UMLS CUI [1,3]
    C1948029
    UMLS CUI [1,4]
    C0178913

    Similar models

    Pharmacogenetic research Withdrawal of consent Subject Identification GSK study Chronic Coronary Heart Disease NCT00799903

    Name
    genere
    Description | Question | Decode (Coded Value)
    Tipo di dati
    Alias
    Item Group
    Withdrawal of consent for PGx (DNA) / Blood sample destruction
    withdrawal consent for PGx research
    Item
    1. Has subject withdrawn consent for PGx research?
    boolean
    C0021430 (UMLS CUI [1,1])
    C2347500 (UMLS CUI [1,2])
    date informed consent withdrawn
    Item
    If subject has withdrawn consent for PGx research: date informed consent withdrawn
    date
    C2985782 (UMLS CUI [1])
    request for blood sample destruction
    Item
    2. Has a request been made for blood sample destruction?
    boolean
    C1948029 (UMLS CUI [1,1])
    C0178913 (UMLS CUI [1,2])
    C1272683 (UMLS CUI [1,3])
    Item
    If a request has been made for blood sample destruction, check reason
    text
    C1948029 (UMLS CUI [1,1])
    C0178913 (UMLS CUI [1,2])
    C0392360 (UMLS CUI [1,3])
    Code List
    If a request has been made for blood sample destruction, check reason
    CL Item
    Subject withdrew consent for PGx (3)
    C1707492 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Other (Z)
    (Comment:en)
    request for blood sample destruction other reason
    Item
    If other reason applied, specify
    text
    C0566251 (UMLS CUI [1,1])
    C1272683 (UMLS CUI [1,2])
    C1948029 (UMLS CUI [1,3])
    C0178913 (UMLS CUI [1,4])

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