The study aims to determine the pharmacodynamic performance in the first hour measured with verifynow, of the conventional ticagrelor loaded dose versus chewed ticagrelor in patients with acute coronary syndrome treated with percutaneous coronary intervention
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
50
Chewed ticagrelor (Brilinta) 90 mg tablets, 2 tablets
Swallowed ticagrelor (Brilinta) 90 mg tablets, 2 tablets
Hospital La Concepción
Saltillo, Coahuila, Mexico
RECRUITINGPlatelet reactivity
Platelet reactivity measured with VerifyNow (PRU)
Time frame: 1 hour
Efficacy (MACCE)
Composite outcome: made by major adverse cardiac and cerebrovascular events: all-cause death, repeat myocardial revascularization, stroke, myocardial infarction
Time frame: 30 days
Composite outcome
Composite outcome: major bleeding, AND nonmajor clinically relevant (NMCR) bleeding both by ISTH definition
Time frame: 30 days
Efficacy (long term)
Composite outcome: number of participants with major adverse cardiac and cerebrovascular events (MACCE) (previously defined)
Time frame: 1 year
High platelet reactivity on treatment rate
Inhibition of platelet aggregation (IPA) measured by VerifyNow
Time frame: 1 hour
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.