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ID

28408

Beschrijving

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

Trefwoorden

Versies (4)
  1. 10-10-17 10-10-17 -
  2. 16-10-17 16-10-17 -
  3. 23-10-17 23-10-17 -
  4. 11-01-18 11-01-18 -
Houder van rechten

GlaxoSmithKline

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11 januari 2018

DOI

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

    Engels

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

    1 Formulieren  
    Assessment date
    Beschrijving

    Assessment date

    1. Most recent survival status assessment
    Beschrijving

    Most recent survival status assessment

    Datatype

    date

    Alias
    UMLS CUI [1,1]
    C2985720
    UMLS CUI [1,2]
    C3846084
    Survival data
    Beschrijving

    Survival data

    1. Subject status
    Beschrijving

    Subject status

    Datatype

    integer

    Alias
    UMLS CUI [1]
    C2348568
    If subject known to be alive: Subject known to be alive on (date)
    Beschrijving

    Date Subject known to be alive

    Datatype

    date

    Alias
    UMLS CUI [1,1]
    C3274947
    UMLS CUI [1,2]
    C0805839
    If subject known to be alive: Source of information
    Beschrijving

    Subject alive Source of information

    Datatype

    text

    Alias
    UMLS CUI [1]
    C0807975
    If subject known to be alive: Other source of information, specify
    Beschrijving

    Subject alive Source of information specification

    Datatype

    text

    Alias
    UMLS CUI [1,1]
    C2584946
    UMLS CUI [1,2]
    C0807975
    If subject died: date that site acquired death information
    Beschrijving

    date that site acquired death information

    Datatype

    date

    Alias
    UMLS CUI [1,1]
    C1306577
    UMLS CUI [1,2]
    C1533716
    If subject died: Source of information
    Beschrijving

    death of subject Source of information

    Datatype

    text

    Alias
    UMLS CUI [1,1]
    C0011065
    UMLS CUI [1,2]
    C1955348
    If subject died: Other source of information, specify
    Beschrijving

    Subject dead Source of information specification

    Datatype

    text

    Alias
    UMLS CUI [1,1]
    C0011065
    UMLS CUI [1,2]
    C1955348
    UMLS CUI [1,3]
    C2348235
    Terug naar het begin van de pagina

    Similar models

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

    1 Formulieren
    Name
    Type
    Description | Question | Decode (Coded Value)
    Datatype
    Alias
    Item Group
    Assessment date
    Most recent survival status assessment
    Item
    1. Most recent survival status assessment
    date
    C2985720 (UMLS CUI [1,1])
    C3846084 (UMLS CUI [1,2])
    Item Group
    Survival data
    Item
    1. Subject status
    integer
    C2348568 (UMLS CUI [1])
    Subject status
    Code List
    1. Subject status
    CL Item
    Subject known to be alive (1)
    C2584946 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Subject died (2)
    C0011065 (UMLS CUI-1)
    (Comment:en)
    Date Subject known to be alive
    Item
    If subject known to be alive: Subject known to be alive on (date)
    date
    C3274947 (UMLS CUI [1,1])
    C0805839 (UMLS CUI [1,2])
    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
    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
    Publicly available information (3)
    C1955348 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Other (OT)
    C0205394 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Investigative site staff (4)
    C0018724 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Friend or neighbor (5)
    C0079382 (UMLS CUI-1)
    (Comment:en)
    Subject alive Source of information specification
    Item
    If subject known to be alive: Other source of information, specify
    text
    C2584946 (UMLS CUI [1,1])
    C0807975 (UMLS CUI [1,2])
    date that site acquired death information
    Item
    If subject died: date that site acquired death information
    date
    C1306577 (UMLS CUI [1,1])
    C1533716 (UMLS CUI [1,2])
    Item
    If subject died: Source of information
    text
    C0011065 (UMLS CUI [1,1])
    C1955348 (UMLS CUI [1,2])
    Subject alive Source of information
    Code List
    If subject died: Source of information
    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
    Publicly available information (3)
    C1955348 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Other (OT)
    C0205394 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Investigative site staff (4)
    C0018724 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Friend or neighbor (5)
    C0079382 (UMLS CUI-1)
    (Comment:en)
    Subject dead Source of information specification
    Item
    If subject died: Other source of information, specify
    text
    C0011065 (UMLS CUI [1,1])
    C1955348 (UMLS CUI [1,2])
    C2348235 (UMLS CUI [1,3])
    Terug naar het begin van de pagina 

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