Switching From Dual Antiplatelet Therapy to Monotherapy With Potent P2Y12 Inhibitors

PHASE4RecruitingINTERVENTIONAL
Enrollment

48

Participants

Timeline

Start Date

January 8, 2025

Primary Completion Date

August 31, 2026

Study Completion Date

December 31, 2026

Conditions
Coronary Artery Disease
Interventions
DRUG

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.

DRUG

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.

Trial Locations (1)

32209

RECRUITING

University of Florida Jacksonville, Jacksonville

All Listed Sponsors
lead

University of Florida

OTHER