Last updated: October 3, 2018
Sponsor: Ottawa Heart Institute Research Corporation
Overall Status: Completed
Phase
2/3
Condition
Myocardial Ischemia
Open Heart Surgery
Chest Pain
Treatment
N/AClinical Study ID
NCT02044146
20130601
Ages 18-75 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Patients: age >18 yrs, < 75yrs
-> 60 kg ( since March 2015 age >75 and < 60 kg eligible - but prasugrel reduced to 5mg daily if randomized to personalized therapy arm)
- NSTEMI undergoing PCI will be eligible
Exclusion
Exclusion Criteria:
- Patients will be excluded if they have: i) a contra-indication for clopidogrel orprasugrel or ticagrelor (as per monograph), ii) have an intolerance to aspirin, iii) haveabsolute requirement for ticagrelor or prasugrel (e.g. stent thrombosis, allergic reactionto clopidogrel), iv) requirement for anti-coagulation treatment, v) a history of stroke,TIA or intracranial hemorrhage , vi) a platelet count < 100,000/μl, vii) a known bleedingdiathesis, viii) hematocrit <30% or >52%, ix) severe liver dysfunction, x) renalinsufficiency (creatinine clearance < 30ml/min), xi) adjuvant therapy with a glycoproteinIIbIIIa inhibitor.
Study Design
Total Participants: 120
Study Start date:
September 01, 2014
Estimated Completion Date:
June 30, 2017
Connect with a study center
University of Ottawa Heart Institute
Ottawa, Ontario K1Y4W7
CanadaSite Not Available
Montreal Heart Institute
Montreal, Quebec H1T1C8
CanadaSite Not Available
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