0 Bedömningar

ID

26720

Beskrivning

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

Nyckelord

  1. 2017-10-09 2017-10-09 -
  2. 2017-10-16 2017-10-16 -
  3. 2017-10-23 2017-10-23 -
  4. 2018-01-11 2018-01-11 -
Rättsinnehavare

GlaxoSmithKline

Uppladdad den

23 oktober 2017

DOI

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Licens

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
    Beskrivning

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

    1. Has subject withdrawn consent for PGx research?
    Beskrivning

    withdrawal consent for PGx research

    Datatyp

    boolean

    If subject has withdrawn consent for PGx research: date informed consent withdrawn
    Beskrivning

    date informed consent withdrawn

    Datatyp

    date

    2. Has a request been made for blood sample destruction?
    Beskrivning

    request for blood sample destruction

    Datatyp

    boolean

    If a request has been made for blood sample destruction, check reason
    Beskrivning

    request for blood sample destruction reason

    Datatyp

    text

    If other reason applied, specify
    Beskrivning

    request for blood sample destruction other reason

    Datatyp

    text

    Similar models

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

    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datatyp
    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 Has subject withdrawn consent for PGx research?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
    date informed consent withdrawn
    Item
    If subject has withdrawn consent for PGx research: date informed consent withdrawn
    date
    request for blood sample destruction
    Item
    2. Has a request been made for blood sample destruction?
    boolean
    Item
    If a request has been made for blood sample destruction, check reason
    text
    Code List
    If a request has been made for blood sample destruction, check reason
    CL Item
    Subject withdrew consent for PGx (3)
    CL Item
    Other (Z)
    request for blood sample destruction other reason
    Item
    If other reason applied, specify
    text

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