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ID

28280

Descrizione

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 contact

Keywords

versioni (3)
  1. 13/10/17 13/10/17 -
  2. 23/10/17 23/10/17 -
  3. 02/01/18 02/01/18 -
Titolare del copyright

GlaxoSmithKline

Caricato su

2 gennaio 2018

DOI

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Licenza

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

    Inglese

    End of study contact GSK study Chronic Coronary Heart Disease NCT00799903

    1 moduli  
    End of study contact form
    Descrizione

    End of study contact form

    1. Was subject contacted?
    Descrizione

    Please select No if continued attempts to contact subject have failed and 3 month EOS period had come to an end. If contact only made with Third party designee instead of subject please complete a THIRD PARTY form.

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1,1]
    C0332158 (Contact with)
    SNOMED
    11723008
    UMLS CUI [1,2]
    C0681850 (Study Subject)
    Type of contact
    Descrizione

    Type of contact

    Tipo di dati

    integer

    Alias
    UMLS CUI [1]
    C0332158 (Contact with)
    SNOMED
    11723008
    If telephone: Time of contact
    Descrizione

    Time of contact

    Tipo di dati

    time

    Alias
    UMLS CUI [1]
    C0805839 (Date last contact)
    LOINC
    MTHU010432
    If telephone: Site staff who conducted call
    Descrizione

    ensure documented in source notes

    Tipo di dati

    text

    Alias
    UMLS CUI [1]
    C0302186 (Telephone Call)
    If telephone: Reason why visit was not perfomed in the clinic
    Descrizione

    Reason visit was not perfomed in clinic

    Tipo di dati

    text

    Alias
    UMLS CUI [1,1]
    C0566251 (Reason and justification)
    SNOMED
    288830005
    UMLS CUI [1,2]
    C3838685 (Medical day care clinic)
    SNOMED
    702881000
    Other, specify
    Descrizione

    Reason visit was not perfomed in clinic specification

    Tipo di dati

    text

    Alias
    UMLS CUI [1,1]
    C0566251 (Reason and justification)
    SNOMED
    288830005
    UMLS CUI [1,2]
    C3838685 (Medical day care clinic)
    SNOMED
    702881000
    Ritorna all'inizio della pagina

    Similar models

    End of study contact GSK study Chronic Coronary Heart Disease NCT00799903

    1 moduli
    Name
    genere
    Description | Question | Decode (Coded Value)
    Tipo di dati
    Alias
    Item Group
    End of study contact form
    subject contact
    Item
    1. Was subject contacted?
    boolean
    C0332158 (UMLS CUI [1,1])
    C0681850 (UMLS CUI [1,2])
    Item
    Type of contact
    integer
    C0332158 (UMLS CUI [1])
    Type of contact
    Code List
    Type of contact
    CL Item
    Clinic visit (1)
    C0008952 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Telephone (2)
    C1515258 (UMLS CUI-1)
    (Comment:en)
    Time of contact
    Item
    If telephone: Time of contact
    time
    C0805839 (UMLS CUI [1])
    Item
    If telephone: Site staff who conducted call
    text
    C0302186 (UMLS CUI [1])
    Site staff who conducted call
    Code List
    If telephone: Site staff who conducted call
    CL Item
    Physician (34)
    C0031831 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Nurse (35)
    C0028661 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Other (OT)
    C0205394 (UMLS CUI-1)
    (Comment:en)
    Item
    If telephone: Reason why visit was not perfomed in the clinic
    text
    C0566251 (UMLS CUI [1,1])
    C3838685 (UMLS CUI [1,2])
    Reason visit was not perfomed in clinic
    Code List
    If telephone: Reason why visit was not perfomed in the clinic
    CL Item
    Subject refused (1)
    C1705116 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Subject not able to visit clinic (2)
    C3838685 (UMLS CUI-1)
    C0545082 (UMLS CUI-2)
    (Comment:en)
    CL Item
    Other (OT)
    (Comment:en)
    Reason visit was not perfomed in clinic specification
    Item
    Other, specify
    text
    C0566251 (UMLS CUI [1,1])
    C3838685 (UMLS CUI [1,2])
    Ritorna all'inizio della pagina 

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