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ID

28410

Description

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

Versions (4)
  1. 10/9/17 10/9/17 -
  2. 10/16/17 10/16/17 -
  3. 10/23/17 10/23/17 -
  4. 1/11/18 1/11/18 -
Copyright Holder

GlaxoSmithKline

Uploaded on

January 11, 2018

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License

Creative Commons BY-NC 3.0
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    Pharmacogenetic research Withdrawal of consent GSK study Chronic Coronary Heart Disease NCT00799903

    English

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

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

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

    1. Has subject withdrawn consent for PGx research?
    Description

    withdrawal consent for PGx research

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0021430 (Informed Consent)
    UMLS CUI [1,2]
    C2347500 (Pharmacogenetic Test)
    If subject has withdrawn consent for PGx research: date informed consent withdrawn
    Description

    date informed consent withdrawn

    Data type

    date

    Alias
    UMLS CUI [1]
    C2985782 (Informed Consent Date)
    2. Has a request been made for blood sample destruction?
    Description

    request for blood sample destruction

    Data type

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

    request for blood sample destruction reason

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C1948029 (Destruction (action))
    UMLS CUI [1,2]
    C0178913 (Blood specimen)
    SNOMED
    119297000
    UMLS CUI [1,3]
    C0392360 (Indication of (contextual qualifier))
    SNOMED
    230165009
    LOINC
    MTHU008319
    If other reason applied, specify
    Description

    request for blood sample destruction other reason

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C0566251 (Reason and justification)
    SNOMED
    288830005
    UMLS CUI [1,2]
    C1272683 (Request - action)
    SNOMED
    385644000
    UMLS CUI [1,3]
    C1948029 (Destruction (action))
    UMLS CUI [1,4]
    C0178913 (Blood specimen)
    SNOMED
    119297000
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    Similar models

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

    1 forms
    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    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])
    undefined item
    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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