0 Bedömningar
ID

28281

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: Third party survival status

Nyckelord

Versioner (5)
  1. 2017-10-12 2017-10-12 -
  2. 2017-10-16 2017-10-16 -
  3. 2017-10-23 2017-10-23 -
  4. 2018-01-02 2018-01-02 -
  5. 2018-01-02 2018-01-02 -
Rättsinnehavare

GlaxoSmithKline

Uppladdad den

2 januari 2018

DOI

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Licens

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

    Engelsk

    Third party survival status GSK study Chronic Coronary Heart Disease NCT00799903

    1 Formulär  
    Assessment date
    Beskrivning

    Assessment date

    1. Most recent survival status assessment
    Beskrivning

    Most recent survival status assessment date

    Datatyp

    date

    Alias
    UMLS CUI [1]
    C3846084 (undefined)
    Survival data
    Beskrivning

    Survival data

    2. Subject status
    Beskrivning

    Subject status

    Datatyp

    integer

    Alias
    UMLS CUI [1]
    C2348568 (Study Subject Participation Status)
    If subject known to be alive: Subject known to be alive on (date):
    Beskrivning

    Subject known to be alive date

    Datatyp

    date

    Alias
    UMLS CUI [1]
    C3274947 (Last Time Seen Alive)
    If subject known to be alive: Source of information
    Beskrivning

    Subject alive Source of information

    Datatyp

    text

    Alias
    UMLS CUI [1]
    C0807975 (Source of follow-up information)
    LOINC
    MTHU010435
    Other source of information, specify
    Beskrivning

    Subject alive Other Source of information

    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

    Subject dead Source of information

    Datatyp

    text

    Other source of information, specify
    Beskrivning

    Subject dead Other Source of information

    Datatyp

    text

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    Similar models

    Third party survival status GSK study Chronic Coronary Heart Disease NCT00799903

    1 Formulär
    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datatyp
    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
    Tillbaka till toppen 

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