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ID

28296

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 Telephone contact

Trefwoorden

  1. 12-10-17 12-10-17 -
  2. 13-10-17 13-10-17 -
  3. 23-10-17 23-10-17 -
  4. 02-01-18 02-01-18 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

2 januari 2018

DOI

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Licentie

Creative Commons BY-NC 3.0

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    End of study Telephone contact GSK study Chronic Coronary Heart Disease NCT00799903

    End of study Telephone contact GSK study Chronic Coronary Heart Disease NCT00799903

    End of study contact form
    Beschrijving

    End of study contact form

    1. Was subject contacted?
    Beschrijving

    subject contact

    Datatype

    boolean

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

    Type of contact

    Datatype

    integer

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

    Time of contact

    Datatype

    time

    Alias
    UMLS CUI [1]
    C1320531 (Time of arrival of emergency services)
    SNOMED
    405798008
    If telephone: Site staff who conducted call
    Beschrijving

    ensure documented in source notes

    Datatype

    text

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

    Reason visit was not perfomed in clinic

    Datatype

    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
    Beschrijving

    Reason visit was not perfomed in clinic specification

    Datatype

    text

    Alias
    UMLS CUI [1,1]
    C0566251 (Reason and justification)
    SNOMED
    288830005
    UMLS CUI [1,2]
    C3838685 (Medical day care clinic)
    SNOMED
    702881000
    UMLS CUI [1,3]
    C0545082 (Visit)

    Similar models

    End of study Telephone contact GSK study Chronic Coronary Heart Disease NCT00799903

    Name
    Type
    Description | Question | Decode (Coded Value)
    Datatype
    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])
    Code List
    Type of contact
    CL Item
    Clinic visit (1)
    CL Item
    Telephone (2)
    Time of contact
    Item
    If telephone: Time of contact
    time
    C1320531 (UMLS CUI [1])
    Item
    If telephone: Site staff who conducted call
    text
    C0302186 (UMLS CUI [1])
    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
    C0566251 (UMLS CUI [1,1])
    C3838685 (UMLS CUI [1,2])
    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)
    C0205394 (UMLS CUI-1)
    (Comment:en)
    Reason visit was not perfomed in clinic specification
    Item
    Other, specify
    text
    C0566251 (UMLS CUI [1,1])
    C3838685 (UMLS CUI [1,2])
    C0545082 (UMLS CUI [1,3])

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