0 Avaliações
ID

28153

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: Unscheduled visit

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Versões (3)
  1. 21/09/2017 21/09/2017 -
  2. 23/10/2017 23/10/2017 -
  3. 22/12/2017 22/12/2017 -
Titular dos direitos

GlaxoSmithKline

Transferido a

22 de dezembro de 2017

DOI

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Licença

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

    Inglês

    Unscheduled visit GSK study Chronic Coronary Heart Disease NCT00799903

    1 Formulários  
    Status of visit
    Descrição

    Status of visit

    1. Which assessments were performed at this unscheduled visit?
    Descrição

    PK sample collection performed at GSK request for sentinel event

    Tipo de dados

    integer

    Alias
    UMLS CUI [1]
    C0220825
    PK sample collection performed at GSK request for sentinel event
    Descrição

    PK sample collection performed at GSK request for sentinel event

    1. Was a pharmacokinetic blood sample obtained?
    Descrição

    pharmacokinetic blood sample obtained

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1,1]
    C0031328
    UMLS CUI [1,2]
    C0178913
    If yes, date sample taken
    Descrição

    date sample taken

    Tipo de dados

    date

    Alias
    UMLS CUI [1]
    C1302413
    if yes, time sample taken
    Descrição

    time sample taken

    Tipo de dados

    time

    Alias
    UMLS CUI [1,1]
    C0040223
    UMLS CUI [1,2]
    C0200345
    If Yes, date of last investigational product dose prior to PK sample
    Descrição

    date of last investigational product dose

    Tipo de dados

    date

    Alias
    UMLS CUI [1]
    C1762893
    If Yes, time of last investigational product dose prior to PK sample
    Descrição

    time of last investigational product dose

    Tipo de dados

    time

    Alias
    UMLS CUI [1,1]
    C0304229
    UMLS CUI [1,2]
    C0678766
    UMLS CUI [1,3]
    C0011008
    Sample Identifier/Sample Number
    Descrição

    Sample Identifier/Sample Number

    Tipo de dados

    text

    Alias
    UMLS CUI [1]
    C1299222
    Voltar ao início da página

    Similar models

    Unscheduled visit GSK study Chronic Coronary Heart Disease NCT00799903

    1 Formulários
    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de dados
    Alias
    Item Group
    Status of visit
    Item
    1. Which assessments were performed at this unscheduled visit?
    integer
    C0220825 (UMLS CUI [1])
    Assessments
    Code List
    1. Which assessments were performed at this unscheduled visit?
    CL Item
    Vital signs (1)
    C0518766 (UMLS CUI-1)
    (Comment:en)
    CL Item
    ECG (2)
    C1623258 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Lab - blood sample (3)
    C0005834 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Urine dipstick (4)
    C0430370 (UMLS CUI-1)
    (Comment:en)
    CL Item
    PK (5)
    C0022877 (UMLS CUI-1)
    (Comment:en)
    Item Group
    PK sample collection performed at GSK request for sentinel event
    pharmacokinetic blood sample obtained
    Item
    1. Was a pharmacokinetic blood sample obtained?
    boolean
    C0031328 (UMLS CUI [1,1])
    C0178913 (UMLS CUI [1,2])
    date sample taken
    Item
    If yes, date sample taken
    date
    C1302413 (UMLS CUI [1])
    time sample taken
    Item
    if yes, time sample taken
    time
    C0040223 (UMLS CUI [1,1])
    C0200345 (UMLS CUI [1,2])
    date of last investigational product dose
    Item
    If Yes, date of last investigational product dose prior to PK sample
    date
    C1762893 (UMLS CUI [1])
    time of last investigational product dose
    Item
    If Yes, time of last investigational product dose prior to PK sample
    time
    C0304229 (UMLS CUI [1,1])
    C0678766 (UMLS CUI [1,2])
    C0011008 (UMLS CUI [1,3])
    Sample Identifier/Sample Number
    Item
    Sample Identifier/Sample Number
    text
    C1299222 (UMLS CUI [1])
    Voltar ao início da página 

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