drugset / Trial / NCT03182855

Cangrelor vs. Ticagrelor for Early Platelet Inhibition in STEMI

NCT03182855

Phase 4 Unknown 80 enrolled University of Aarhus
RandomizedParallel-groupOpen-labelTreatment

Summary

This randomized, controlled trial compares the anti-thrombotic effect of cangrelor and ticagrelor on platelet activity in patients with acute ST-elevation myocardial infarction. Patients will receive either prehospital ticagrelor (180 mg - crushed) or in-hospital cangrelor (bolus 30 μg/kg within 1 minute followed by infusion (4 μg/kg/minute) for two hours) followed by 180 mg ticagrelor. The primary study end-point is platelet reactivity at sheath insertion, at the end of the PCI procedure (before sheath removal) and two hours after PCI is initiated. The secondary end-point is the proportion of patients with inappropriate or harmful P2Y12 administration.

Timeline

Start
2018-09-01
Primary completion
2019-06-01
Completion
2019-08-01

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Cangrelor Small molecule 4 ug/kg Intravenous
Comparator Ticagrelor Small molecule 180 mg Oral