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ID

28311

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: Pharmacokinetics - Repeating form (Scheduled visits)

Mots-clés

Versions (4)
  1. 05/10/2017 05/10/2017 -
  2. 16/10/2017 16/10/2017 -
  3. 23/10/2017 23/10/2017 -
  4. 03/01/2018 03/01/2018 -
Détendeur de droits

GlaxoSmithKline

Téléchargé le

3 janvier 2018

DOI

Pour une demande vous connecter.

Licence

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

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    Pharmacokinetics GSK study Chronic Coronary Heart Disease NCT00799903

    1 Formulaires  
    An unscheduled PK blood sample must be obtained within 72 hours of last dose
    Description

    An unscheduled PK blood sample must be obtained within 72 hours of last dose

    1. Was a pharmacokinetic blood sample obtained?
    Description

    pharmacokinetic blood sample

    Type de données

    boolean

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

    Date of blood sample

    Type de données

    date

    Alias
    UMLS CUI [1,1]
    C0005834
    UMLS CUI [1,2]
    C0011008
    If yes, time taken
    Description

    Time of blood sample

    Type de données

    time

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

    date of last investigational product dose prior to PK sample

    Type de données

    date

    Alias
    UMLS CUI [1,1]
    C0011008
    UMLS CUI [1,2]
    C0040223
    UMLS CUI [1,3]
    C0678766
    If Yes, time of last investigational product dose prior to PK sample
    Description

    time of last investigational product dose prior to PK sample

    Type de données

    time

    Alias
    UMLS CUI [1,1]
    C0011008
    UMLS CUI [1,2]
    C0040223
    UMLS CUI [1,3]
    C0678766
    Sample Identifier/Sample Number
    Description

    Sample Identifier and Sample Number are conditional. The study team must choose one for inclusion on the eCRF form.

    Type de données

    text

    Alias
    UMLS CUI [1]
    C1299222
    Retour au début de la page

    Similar models

    Pharmacokinetics GSK study Chronic Coronary Heart Disease NCT00799903

    1 Formulaires
    Name
    Type
    Description | Question | Decode (Coded Value)
    Type de données
    Alias
    Item Group
    An unscheduled PK blood sample must be obtained within 72 hours of last dose
    pharmacokinetic blood sample
    Item
    1. Was a pharmacokinetic blood sample obtained?
    boolean
    C0031328 (UMLS CUI [1,1])
    C0178913 (UMLS CUI [1,2])
    Date of blood sample
    Item
    If yes, date taken
    date
    C0005834 (UMLS CUI [1,1])
    C0011008 (UMLS CUI [1,2])
    Time of blood sample
    Item
    If yes, time taken
    time
    C0200345 (UMLS CUI [1,1])
    C0040223 (UMLS CUI [1,2])
    date of last investigational product dose prior to PK sample
    Item
    If Yes, date of last investigational product dose prior to PK sample
    date
    C0011008 (UMLS CUI [1,1])
    C0040223 (UMLS CUI [1,2])
    C0678766 (UMLS CUI [1,3])
    time of last investigational product dose prior to PK sample
    Item
    If Yes, time of last investigational product dose prior to PK sample
    time
    C0011008 (UMLS CUI [1,1])
    C0040223 (UMLS CUI [1,2])
    C0678766 (UMLS CUI [1,3])
    Sample Identifier/Sample Number
    Item
    Sample Identifier/Sample Number
    text
    C1299222 (UMLS CUI [1])
    Retour au début de la page 

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