ID

26739

Description

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

Mots-clés

Versions (3)
  1. 13/10/2017 13/10/2017 -
  2. 23/10/2017 23/10/2017 -
  3. 02/01/2018 02/01/2018 -
Détendeur de droits

GlaxoSmithKline

Téléchargé le

23 octobre 2017

DOI

Pour une demande vous connecter.

Licence

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

Anglais

End of study contact GSK study Chronic Coronary Heart Disease NCT00799903

1 Formulaires  
End of study contact form
Description

End of study contact form

1. Was subject contacted?
Description

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.

Type de données

boolean

Type of contact
Description

Type of contact

Type de données

integer

If telephone: Time of contact
Description

Time of contact

Type de données

time

If telephone: Site staff who conducted call
Description

ensure documented in source notes

Type de données

text

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

Reason visit was not perfomed in clinic

Type de données

text

Other, specify
Description

Reason visit was not perfomed in clinic specification

Type de données

text

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Similar models

End of study contact GSK study Chronic Coronary Heart Disease NCT00799903

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
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
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