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26341

Beschreibung

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: Survival

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GlaxoSmithKline

Hochgeladen am

16. Oktober 2017

DOI

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Creative Commons BY-NC 3.0
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    Survival GSK study Chronic Coronary Heart Disease NCT00799903

    Englisch

    Survival Identification GSK study Chronic Coronary Heart Disease NCT00799903

    1 Formulare  
    Survival data
    Beschreibung

    Survival data

    1. Subject status
    Beschreibung

    Subject status

    Datentyp

    integer

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

    Date Subject known to be alive

    Datentyp

    date

    If subject known to be alive: Source of information
    Beschreibung

    Subject alive Source of information

    Datentyp

    text

    If subject died: date that site acquired death information
    Beschreibung

    date that site acquired death information

    Datentyp

    date

    If subject died: Source of information
    Beschreibung

    death of subject Source of information

    Datentyp

    text

    If no new Survival Status data available: Date of most recent attempt to assess survival status
    Beschreibung

    Date of most recent attempt to assess survival status

    Datentyp

    date

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    Ähnliche Modelle

    Survival Identification GSK study Chronic Coronary Heart Disease NCT00799903

    1 Formulare
    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datentyp
    Alias
    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)
    CL Item
    No new Survival Status data available for this subject since the last data were collected (3)
    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 (e.g., newspaper, newsletter, featured in a performance, award, or interview, etc) (3)
    CL Item
    Other (OT)
    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 (e.g., newspaper, newsletter, featured in a performance, award, or interview, etc) (3)
    CL Item
    Other (OT)
    Date of most recent attempt to assess survival status
    Item
    If no new Survival Status data available: Date of most recent attempt to assess survival status
    date
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