0 Avaliações
ID

28290

Descrição

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

Palavras-chave

Versões (5)
  1. 12/10/2017 12/10/2017 -
  2. 16/10/2017 16/10/2017 -
  3. 23/10/2017 23/10/2017 -
  4. 02/01/2018 02/01/2018 -
  5. 02/01/2018 02/01/2018 -
Titular dos direitos

GlaxoSmithKline

Transferido a

2 de janeiro de 2018

DOI

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Licença

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

    Inglês

    Third party survival status GSK study Chronic Coronary Heart Disease NCT00799903

    1 Formulários  
    Assessment date
    Descrição

    Assessment date

    1. Most recent survival status assessment
    Descrição

    Most recent survival status assessment date

    Tipo de dados

    date

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

    Survival data

    2. Subject status
    Descrição

    Subject status

    Tipo de dados

    integer

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

    Subject known to be alive date

    Tipo de dados

    date

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

    Subject alive Source of information

    Tipo de dados

    text

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

    Subject alive Other Source of information

    Tipo de dados

    text

    Alias
    UMLS CUI [1,1]
    C0027361 (Persons)
    SNOMED
    125676002
    UMLS CUI [1,2]
    C0449416 (Source)
    SNOMED
    260753009
    LOINC
    LP21212-3
    UMLS CUI [1,3]
    C1533716 (Information)
    UMLS CUI [1,4]
    C0038952 (Continuance of life)
    If subject died: date that site acquired death information
    Descrição

    Date that site acquired death information

    Tipo de dados

    date

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

    Subject dead Source of information

    Tipo de dados

    text

    Alias
    UMLS CUI [1,1]
    C0683836 (Source of information)
    SNOMED
    385438008
    UMLS CUI [1,2]
    C0011065 (Cessation of life)
    SNOMED
    419620001
    Other source of information, specify
    Descrição

    Subject dead Other Source of information

    Tipo de dados

    text

    Alias
    UMLS CUI [1,1]
    C0683836 (Source of information)
    SNOMED
    385438008
    UMLS CUI [1,2]
    C0011065 (Cessation of life)
    SNOMED
    419620001
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    Similar models

    Third party survival status GSK study Chronic Coronary Heart Disease NCT00799903

    1 Formulários
    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de dados
    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)
    C2584946 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Subject died (2)
    C0011065 (UMLS CUI-1)
    (Comment:en)
    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)
    Subject alive Other Source of information
    Item
    Other source of information, specify
    text
    C0027361 (UMLS CUI [1,1])
    C0449416 (UMLS CUI [1,2])
    C1533716 (UMLS CUI [1,3])
    C0038952 (UMLS CUI [1,4])
    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
    C0683836 (UMLS CUI [1,1])
    C0011065 (UMLS CUI [1,2])
    Subject alive Source of information
    Code List
    If subject died: Source of information
    CL Item
    Investigative site staff (4)
    (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)
    C0079382 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Publicly available information (3)
    C1955348 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Other (OT)
    (Comment:en)
    Subject dead Other Source of information
    Item
    Other source of information, specify
    text
    C0683836 (UMLS CUI [1,1])
    C0011065 (UMLS CUI [1,2])
    Voltar ao início da página 

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