De-escalating Antiplatelet Therapy to Assess Platelet Reactivity and Outcomes in High Bleeding Risk Patients With Recent ACS

PHASE3RecruitingINTERVENTIONAL
Enrollment

200

Participants

Timeline

Start Date

June 12, 2023

Primary Completion Date

June 30, 2025

Study Completion Date

October 30, 2025

Conditions
Dual Antiplatelet TherapyAcute Coronary SyndromeCoronary Artery Disease
Interventions
DRUG

P2Y12 inhibitor de-escalation

Comparing, in patients at High Bleeding Risk (HBR) after a recent Acute Coronary Syndrome (ACS), continuation of full-dose potent P2Y12 inhibitor with a P2Y12i de-escalation strategy transitioning to clopidogrel 75mg, prasugrel 5mg or ticagrelor 60mg/bid.

Trial Locations (2)

10098

NOT_YET_RECRUITING

Ospedale degli Infermi, Rivoli

98125

RECRUITING

Azienda Ospedaliera Universitaria Gaetano Martino, Messina

All Listed Sponsors
collaborator

Giampiero Vizzari

UNKNOWN

collaborator

Giorgio Quadri

UNKNOWN

collaborator

Greca Zanda

UNKNOWN

collaborator

Ferdinando Varbella

UNKNOWN

collaborator

Gianluca Di Bella

UNKNOWN

collaborator

Antonio Micari

UNKNOWN

lead

"Azienda Ospedaliera Universitaria Policlinico G. Martino"

OTHER

NCT05903976 - De-escalating Antiplatelet Therapy to Assess Platelet Reactivity and Outcomes in High Bleeding Risk Patients With Recent ACS | Biotech Hunter | Biotech Hunter