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RECRUITING
NCT07025148
PHASE4

Dual Antiplatelet Therapy Escalation From Standard-dose Clopidogrel to Low-Dose Prasugrel in Patients With High Bleeding and Ischemic Risk Undergoing PCI: A Prospective, Randomized Pharmacodynamic Study (TAILOR-BLEED-2)

Sponsor: University of Florida

View on ClinicalTrials.gov

Summary

The primary aim of this study is to investigate the PD effects of switching from standard-dose clopidogrel dose to low-dose prasugrel versus continuing standard-dose clopidogrel in patients at dual-risk (HBR defined as the HBR-ARC criteria and HIR defined as ABCD-GENE score ≥10) following PCI. We hypothesize that in patients at dual-risk, switching from standard-dose clopidogrel to low-dose prasugrel will be superior to continuing standard-dose clopidogrel in terms of platelet reactivity.

Official title: Switching From Clopidogrel to Low-dose Prasugrel in Patients at Dual-risk Following Percutaneous Coronary Intervention (TAILOR-BLEED-2)

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

40

Start Date

2025-10-01

Completion Date

2027-11-01

Last Updated

2025-11-04

Healthy Volunteers

No

Interventions

DRUG

Prasugrel

Prasugrel 5 mg od for 30 ± 5 days

DRUG

Clopidogrel

Clopidogrel 75 mg od for 30 ± 5 days

Locations (1)

University of Florida Health

Jacksonville, Florida, United States