0 Ratings
ID

26722

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

Versions (4)
  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

October 23, 2017

DOI

To request one please log in.

License

Creative Commons BY-NC 3.0
Model comments :

You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.

Back to model comments
Itemgroup comments for :

Item comments for :

  • Newest
  • Oldest
  • Popular
  • Newest
    • Newest
    • Oldest
    • Popular

    No comments

    In order to download data models you must be logged in. Please log in or register for free.

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

    English

    End of study 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

    Data type

    date

    Survival data
    Description

    Survival data

    1. Subject status
    Description

    Subject status

    Data type

    integer

    If subject known to be alive: Subject known to be alive on (date)
    Description

    Date Subject known to be alive

    Data type

    date

    If subject known to be alive: Source of information
    Description

    Subject alive Source of information

    Data type

    text

    If subject known to be alive: Other source of information, specify
    Description

    Subject alive Source of information specification

    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

    death of subject Source of information

    Data type

    text

    If subject died: Other source of information, specify
    Description

    Subject dead Source of information specification

    Data type

    text

    Back to the top of the page

    Similar models

    End of study 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
    Item
    1. Most recent survival status assessment
    date
    Item Group
    Survival data
    Item
    1. Subject status
    integer
    Subject status
    Code List
    1. Subject status
    CL Item
    Subject known to be alive (1)
    CL Item
    Subject died (2)
    Date Subject known to be alive
    Item
    If subject known to be alive: Subject known to be alive on (date)
    date
    Item
    If subject known to be alive: Source of information
    text
    Subject alive Source of information
    Code List
    If subject known to be alive: Source of information
    CL Item
    Health care provider other than investigative site staff (1)
    CL Item
    Family member (2)
    CL Item
    Publicly available information (3)
    CL Item
    Other (OT)
    CL Item
    Investigative site staff (4)
    CL Item
    Friend or neighbor (5)
    Item
    If subject known to be alive: Other source of information, specify
    text
    Subject alive Source of information
    Code List
    If subject known to be alive: 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
    Health care provider other than investigative site staff (1)
    CL Item
    Family member (2)
    CL Item
    Publicly available information (3)
    CL Item
    Other (OT)
    CL Item
    Investigative site staff (4)
    CL Item
    Friend or neighbor (5)
    Subject dead Source of information specification
    Item
    If subject died: Other source of information, specify
    text
    Back to the top of the page 

    Help

    Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

    Watch Tutorial