Randomised trial comparing the effectiveness of ticagrelor and prasugrel in patients with ST segment elevation myocardial infarction (STEMI) who have been treated with primary PCI.
start of the project: October 2013
The randomised multicentre trial Prague 18 involves patients with acute myocardial infarction who have been indicated for primary percutaneous coronary intervention (PCI). Patients are subsequently randomised into one of the following treatment arms. Arm 1: Patients receive prasugrel at a loading dose of 60 mg and a maintenance dose of 10(5) mg/day. Arm 2: Patients receive ticagrelor at a loading dose of 180 mg and a maintenance dose of twice 90 mg/day.