ID

28408

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: End of study Survival status

Keywords

  1. 10/10/17 10/10/17 -
  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

DOI

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License

Creative Commons BY-NC 3.0

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    End of study Survival status GSK study Chronic Coronary Heart Disease NCT00799903

    End of study Survival status GSK study Chronic Coronary Heart Disease NCT00799903

    Assessment date
    Description

    Assessment date

    1. Most recent survival status assessment
    Description

    Most recent survival status assessment

    Data type

    date

    Alias
    UMLS CUI [1,1]
    C2985720
    UMLS CUI [1,2]
    C3846084
    Survival data
    Description

    Survival data

    1. Subject status
    Description

    Subject status

    Data type

    integer

    Alias
    UMLS CUI [1]
    C2348568
    If subject known to be alive: Subject known to be alive on (date)
    Description

    Date Subject known to be alive

    Data type

    date

    Alias
    UMLS CUI [1,1]
    C3274947
    UMLS CUI [1,2]
    C0805839
    If subject known to be alive: Source of information
    Description

    Subject alive Source of information

    Data type

    text

    Alias
    UMLS CUI [1]
    C0807975
    If subject known to be alive: Other source of information, specify
    Description

    Subject alive Source of information specification

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C2584946
    UMLS CUI [1,2]
    C0807975
    If subject died: date that site acquired death information
    Description

    date that site acquired death information

    Data type

    date

    Alias
    UMLS CUI [1,1]
    C1306577
    UMLS CUI [1,2]
    C1533716
    If subject died: Source of information
    Description

    death of subject Source of information

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C0011065
    UMLS CUI [1,2]
    C1955348
    If subject died: Other source of information, specify
    Description

    Subject dead Source of information specification

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C0011065
    UMLS CUI [1,2]
    C1955348
    UMLS CUI [1,3]
    C2348235

    Similar models

    End of study Survival status GSK study Chronic Coronary Heart Disease NCT00799903

    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    Assessment date
    Most recent survival status assessment
    Item
    1. Most recent survival status assessment
    date
    C2985720 (UMLS CUI [1,1])
    C3846084 (UMLS CUI [1,2])
    Item Group
    Survival data
    Item
    1. Subject status
    integer
    C2348568 (UMLS CUI [1])
    Code List
    1. Subject status
    CL Item
    Subject known to be alive (1)
    C2584946 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Subject died (2)
    C0011065 (UMLS CUI-1)
    (Comment:en)
    Date Subject known to be alive
    Item
    If subject known to be alive: Subject known to be alive on (date)
    date
    C3274947 (UMLS CUI [1,1])
    C0805839 (UMLS CUI [1,2])
    Item
    If subject known to be alive: Source of information
    text
    C0807975 (UMLS CUI [1])
    Code List
    If subject known to be alive: Source of information
    CL Item
    Health care provider other than investigative site staff (1)
    C0018724 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Family member (2)
    C0086282 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Publicly available information (3)
    C1955348 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Other (OT)
    C0205394 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Investigative site staff (4)
    C0018724 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Friend or neighbor (5)
    C0079382 (UMLS CUI-1)
    (Comment:en)
    Subject alive Source of information specification
    Item
    If subject known to be alive: Other source of information, specify
    text
    C2584946 (UMLS CUI [1,1])
    C0807975 (UMLS CUI [1,2])
    date that site acquired death information
    Item
    If subject died: date that site acquired death information
    date
    C1306577 (UMLS CUI [1,1])
    C1533716 (UMLS CUI [1,2])
    Item
    If subject died: Source of information
    text
    C0011065 (UMLS CUI [1,1])
    C1955348 (UMLS CUI [1,2])
    Code List
    If subject died: Source of information
    CL Item
    Health care provider other than investigative site staff (1)
    C0018724 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Family member (2)
    C0086282 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Publicly available information (3)
    C1955348 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Other (OT)
    C0205394 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Investigative site staff (4)
    C0018724 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Friend or neighbor (5)
    C0079382 (UMLS CUI-1)
    (Comment:en)
    Subject dead Source of information specification
    Item
    If subject died: Other source of information, specify
    text
    C0011065 (UMLS CUI [1,1])
    C1955348 (UMLS CUI [1,2])
    C2348235 (UMLS CUI [1,3])

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