This is a two-center, prospective, randomized, single-blind, investigator initiated, pharmacodynamic study of parallel design, carried out in 2 PCI-capable cardiology centers (Patras University Hospital and Konstantopoulio General Hospital of Athens). Patients with ST elevation myocardial infarction, having undergone fibrinolysis in the previous 3 to 48 hours, who present high residual PR (defined as PRU ≥208 ) on admission, pre coronary angiography, will be randomized after written informed consent, in a 1:1 ratio to either: Ticagrelor 180mg loading dose (LD), followed by a 90mg x2 maintenance dose (MD) starting 12±6 hours post LD, until discharge. Or Clopidogrel 600mg loading dose (LD), followed by a 150mg once daily maintenance dose (MD) starting 12±6 hours post LD, until discharge. Platelet reactivity assessment will be performed at randomization (Hour 0) and at 2, 24 hours after randomization, as well as pre-discharge, using the VerifyNow assay, in platelet reactivity units (PRU). Documentation of major adverse cardiac events (death, myocardial infarction, stroke, ischemia driven revascularization procedure with PCI or CABG) and bleeding (according to BARC criteria) will be performed until patient's discharge.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
56
Konstantopoulio General Hospital of Athens
Athens, Attica, Greece
Patras University Hospital
Pátrai, Greece
Platelet reactivity at 2 hours post randomization between the 2 treatment arms
Platelet reactivity at 2 hours post randomization between the 2 treatment arms
Time frame: 2 hours
Platelet reactivity at 24 hours post randomization between the 2 treatment arms.
Time frame: 24 hours
Platelet reactivity pre-discharge between the 2 treatment arms
Time frame: 5 days
High on treatment platelet reactivity (HPR) rate (≥208 PRU) at 2 hours post randomization
Time frame: 2 hours
High on treatment platelet reactivity (HPR) rate (≥208 PRU) at 24 hours post randomization
Time frame: 24 hours
High on treatment platelet reactivity (HPR) rates (≥208 PRU) pre discharge
Time frame: 5 days
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