0 Bedömningar

ID

26722

Beskrivning

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

Nyckelord

  1. 2017-10-10 2017-10-10 -
  2. 2017-10-16 2017-10-16 -
  3. 2017-10-23 2017-10-23 -
  4. 2018-01-11 2018-01-11 -
Rättsinnehavare

GlaxoSmithKline

Uppladdad den

23 oktober 2017

DOI

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Licens

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
    Beskrivning

    Assessment date

    1. Most recent survival status assessment
    Beskrivning

    Most recent survival status assessment

    Datatyp

    date

    Survival data
    Beskrivning

    Survival data

    1. Subject status
    Beskrivning

    Subject status

    Datatyp

    integer

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

    Date Subject known to be alive

    Datatyp

    date

    If subject known to be alive: Source of information
    Beskrivning

    Subject alive Source of information

    Datatyp

    text

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

    Subject alive Source of information specification

    Datatyp

    text

    If subject died: date that site acquired death information
    Beskrivning

    date that site acquired death information

    Datatyp

    date

    If subject died: Source of information
    Beskrivning

    death of subject Source of information

    Datatyp

    text

    If subject died: Other source of information, specify
    Beskrivning

    Subject dead Source of information specification

    Datatyp

    text

    Similar models

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

    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datatyp
    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
    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
    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
    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
    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

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