0 Ratings
ID

28281

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: Third party survival status

Keywords

Versions (5)
  1. 10/12/17 10/12/17 -
  2. 10/16/17 10/16/17 -
  3. 10/23/17 10/23/17 -
  4. 1/2/18 1/2/18 -
  5. 1/2/18 1/2/18 -
Copyright Holder

GlaxoSmithKline

Uploaded on

January 2, 2018

DOI

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License

Creative Commons BY-NC 3.0
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    Third party survival status GSK study Chronic Coronary Heart Disease NCT00799903

    English

    Third party survival status GSK study Chronic Coronary Heart Disease NCT00799903

    1 forms  
    Assessment date
    Description

    Assessment date

    1. Most recent survival status assessment
    Description

    Most recent survival status assessment date

    Data type

    date

    Alias
    UMLS CUI [1]
    C3846084
    Survival data
    Description

    Survival data

    2. 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

    Subject known to be alive date

    Data type

    date

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

    Subject alive Source of information

    Data type

    text

    Alias
    UMLS CUI [1]
    C0807975
    Other source of information, specify
    Description

    Subject alive Other Source of information

    Data type

    text

    If subject died: date that site acquired death information
    Description

    Date that site acquired death information

    Data type

    date

    If subject died: Source of information
    Description

    Subject dead Source of information

    Data type

    text

    Other source of information, specify
    Description

    Subject dead Other Source of information

    Data type

    text

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    Similar models

    Third party survival status GSK study Chronic Coronary Heart Disease NCT00799903

    1 forms
    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    Assessment date
    Most recent survival status assessment date
    Item
    1. Most recent survival status assessment
    date
    C3846084 (UMLS CUI [1])
    Item Group
    Survival data
    Item
    2. Subject status
    integer
    C2348568 (UMLS CUI [1])
    Subject status
    Code List
    2. Subject status
    CL Item
    Subject known to be alive (1)
    CL Item
    Subject died (2)
    Subject known to be alive date
    Item
    If subject known to be alive: Subject known to be alive on (date):
    date
    C3274947 (UMLS CUI [1])
    Item
    If subject known to be alive: Source of information
    text
    C0807975 (UMLS CUI [1])
    Subject alive Source of information
    Code List
    If subject known to be alive: Source of information
    CL Item
    Investigative site staff (4)
    C1512698 (UMLS CUI-1)
    C0205197 (UMLS CUI-2)
    C0281588 (UMLS CUI-3)
    (Comment:en)
    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
    Friend or neighbor (5)
    C3842310 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Publicly available information (3)
    C1546437 (UMLS CUI-1)
    C0005957 (UMLS CUI-2)
    (Comment:en)
    CL Item
    Other (OT)
    C0205394 (UMLS CUI-1)
    (Comment:en)
    Item
    Other source of information, specify
    text
    Subject alive Source of information
    Code List
    Other source of information, specify
    Date that site acquired death information
    Item
    If subject died: date that site acquired death information
    date
    Item
    If subject died: Source of information
    text
    Subject alive Source of information
    Code List
    If subject died: Source of information
    CL Item
    Investigative site staff (4)
    CL Item
    Health care provider other than investigative site staff (1)
    CL Item
    Family member (2)
    CL Item
    Friend or neighbor (5)
    CL Item
    Publicly available information (3)
    CL Item
    Other (OT)
    Subject dead Other Source of information
    Item
    Other source of information, specify
    text
    Back to the top of the page 

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