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ID

28409

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: Survival

Mots-clés

Versions (6)
  1. 10/10/2017 10/10/2017 -
  2. 10/10/2017 10/10/2017 -
  3. 16/10/2017 16/10/2017 -
  4. 16/10/2017 16/10/2017 -
  5. 23/10/2017 23/10/2017 -
  6. 11/01/2018 11/01/2018 -
Détendeur de droits

GlaxoSmithKline

Téléchargé le

11 janvier 2018

DOI

Pour une demande vous connecter.

Licence

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

    Anglais

    Survival Identification GSK study Chronic Coronary Heart Disease NCT00799903

    1 Formulaires  
    Survival data
    Description

    Survival data

    1. Subject status
    Description

    Subject status

    Type de données

    integer

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

    Date Subject known to be alive

    Type de données

    date

    Alias
    UMLS CUI [1]
    C2584946 (Alive (finding))
    SNOMED
    438949009
    LOINC
    LA4247-8
    If subject known to be alive: Source of information
    Description

    Subject alive Source of information

    Type de données

    text

    Alias
    UMLS CUI [1]
    C0807975 (Source of follow-up information)
    LOINC
    MTHU010435
    If subject died: date that site acquired death information
    Description

    date that site acquired death information

    Type de données

    date

    Alias
    UMLS CUI [1,1]
    C1306577 (Death (finding))
    LOINC
    LA7424-0
    UMLS CUI [1,2]
    C1533716 (Information)
    If subject died: Source of information
    Description

    death of subject Source of information

    Type de données

    text

    Alias
    UMLS CUI [1,1]
    C0011065 (Cessation of life)
    SNOMED
    419620001
    UMLS CUI [1,2]
    C1955348 (Patient Information)
    If no new Survival Status data available: Date of most recent attempt to assess survival status
    Description

    Date of most recent attempt to assess survival status

    Type de données

    date

    Alias
    UMLS CUI [1]
    C3846084 (undefined)
    Retour au début de la page

    Similar models

    Survival Identification GSK study Chronic Coronary Heart Disease NCT00799903

    1 Formulaires
    Name
    Type
    Description | Question | Decode (Coded Value)
    Type de données
    Alias
    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)
    CL Item
    No new Survival Status data available for this subject since the last data were collected (3)
    C1320722 (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
    C2584946 (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
    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 (e.g., newspaper, newsletter, featured in a performance, award, or interview, etc) (3)
    C1955348 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Other (OT)
    C0205394 (UMLS CUI-1)
    (Comment:en)
    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 (e.g., newspaper, newsletter, featured in a performance, award, or interview, etc) (3)
    C1955348 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Other (OT)
    C0205394 (UMLS CUI-1)
    (Comment:en)
    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
    C3846084 (UMLS CUI [1])
    Retour au début de la page 

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