ID

26241

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

  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

13 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

End of study contact GSK study Chronic Coronary Heart Disease NCT00799903

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

Similar models

End of study 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
Item
Type of contact
integer
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
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
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

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