48
Participants
Start Date
January 8, 2025
Primary Completion Date
August 31, 2026
Study Completion Date
December 31, 2026
Ticagrelor 90 mg
After providing written informed consent, patients on DAPT meeting study entry criteria will stop aspirin and be randomly assigned in a 1:1 fashion using a computer-based randomization system to either: a) ticagrelor 90 mg bid monotherapy or b) prasugrel 10 mg qd monotherapy. Patients will continue the randomized treatment for 21±7 days.
Prasugrel 10 mg
After providing written informed consent, patients on DAPT meeting study entry criteria will stop aspirin and be randomly assigned in a 1:1 fashion using a computer-based randomization system to either: a) ticagrelor 90 mg bid monotherapy or b) prasugrel 10 mg qd monotherapy. Patients will continue the randomized treatment for 21±7 days.
RECRUITING
University of Florida Jacksonville, Jacksonville
University of Florida
OTHER