0 Beoordelingen
ID

28280

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

2 januari 2018

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY-NC 3.0
Model Commentaren :

Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.

Terug naar het model Commentaren
Itemgroep Commentaren voor :

Item Commentaren voor :

  • Nieuwste
  • Oudste
  • Populair
  • Nieuwste
    • Nieuwste
    • Oudste
    • Populair

    Geen commentaren

    U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.

    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

    Alias
    UMLS CUI [1,1]
    C0332158
    UMLS CUI [1,2]
    C0681850
    Type of contact
    Beschrijving

    Type of contact

    Datatype

    integer

    Alias
    UMLS CUI [1]
    C0332158
    If telephone: Time of contact
    Beschrijving

    Time of contact

    Datatype

    time

    Alias
    UMLS CUI [1]
    C0805839
    If telephone: Site staff who conducted call
    Beschrijving

    ensure documented in source notes

    Datatype

    text

    Alias
    UMLS CUI [1]
    C0302186
    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
    UMLS CUI [1,2]
    C3838685
    Other, specify
    Beschrijving

    Reason visit was not perfomed in clinic specification

    Datatype

    text

    Alias
    UMLS CUI [1,1]
    C0566251
    UMLS CUI [1,2]
    C3838685
    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
    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])
    Terug naar het begin van de pagina 

    Help

    Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

    Watch Tutorial