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ID

26739

Beschrijving

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

Trefwoorden

Versies (3)
  1. 13-10-17 13-10-17 -
  2. 23-10-17 23-10-17 -
  3. 02-01-18 02-01-18 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

23 oktober 2017

DOI

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Licentie

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

    Engels

    End of study contact GSK study Chronic Coronary Heart Disease NCT00799903

    1 Formulieren  
    End of study contact form
    Beschrijving

    End of study contact form

    1. Was subject contacted?
    Beschrijving

    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.

    Datatype

    boolean

    Type of contact
    Beschrijving

    Type of contact

    Datatype

    integer

    If telephone: Time of contact
    Beschrijving

    Time of contact

    Datatype

    time

    If telephone: Site staff who conducted call
    Beschrijving

    ensure documented in source notes

    Datatype

    text

    If telephone: Reason why visit was not perfomed in the clinic
    Beschrijving

    Reason visit was not perfomed in clinic

    Datatype

    text

    Other, specify
    Beschrijving

    Reason visit was not perfomed in clinic specification

    Datatype

    text

    Terug naar het begin van de pagina

    Similar models

    End of study contact GSK study Chronic Coronary Heart Disease NCT00799903

    1 Formulieren
    Name
    Type
    Description | Question | Decode (Coded Value)
    Datatype
    Alias
    Item Group
    End of study contact form
    subject contact
    Item
    1. Was subject contacted?
    boolean
    Item
    Type of contact
    integer
    Type of contact
    Code List
    Type of contact
    CL Item
    Clinic visit (1)
    CL Item
    Telephone (2)
    Time of contact
    Item
    If telephone: Time of contact
    time
    Item
    If telephone: Site staff who conducted call
    text
    Site staff who conducted call
    Code List
    If telephone: Site staff who conducted call
    CL Item
    Physician (34)
    CL Item
    Nurse (35)
    CL Item
    Other (OT)
    Item
    If telephone: Reason why visit was not perfomed in the clinic
    text
    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)
    CL Item
    Subject not able to visit clinic (2)
    CL Item
    Other (OT)
    Reason visit was not perfomed in clinic specification
    Item
    Other, specify
    text
    Terug naar het begin van de pagina 

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