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NCT02099422 Clinical Trial

Timing of Optimal Platelet Inhibition After Acute Coronary Syndrome

Acute Coronary Syndrome Clinical Trial

— TOPIC  

Official title:
The Randomized TOPIC Study : Timing of Optimal Platelet Inhibition After Acute Coronary Syndrome

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT02099422
Other study ID # APHM-011
Secondary ID 2013-A01168-37
Status Recruiting
Phase N/A
First received March 26, 2014
Last updated March 26, 2014
Start date January 2013
Est. completion date January 2016

Study information
Verified date March 2014
Source Hôpital de la Timone
Contact thomas cuisset, MD-PHD
Phone 33(0) 491385981
Email thomas.cuisset@ap-hm.fr
Is FDA regulated No
Health authority france : "ANSM"
Study type Observational

Clinical Trial Summary

Comparison of two antiplatelet strategies between months 1 and 12 after coronary stenting for ACS. Efficiency and tolerance évaluation

Recruitment information / eligibility
Status Recruiting
Enrollment 500
Est. completion date January 2016
Est. primary completion date January 2015
Accepts healthy volunteers
Gender Both
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria:

- ACS and coronary stenting one month ago

Exclusion Criteria:

- age under 18 and pregnancy

Study Design

Observational Model: Case Control, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
France CHU Timone hospital . Sc CARDIOLOGIE. Rue saint Pierre. Marseille

Sponsors (1)
Lead Sponsor Collaborator
Hôpital de la Timone

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary combined ischemic and hemorragic endpoint 12 months No
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