drugset / Trial / NCT07846462

Aspirin 50mg vs 100mg Combined With P2Y12 Inhibitor After PCI

NCT07846462 ↗

Recruiting 2640 enrolled Jilin University
RandomizedParallel-groupOpen-labelTreatment

Summary

This is a randomized, open-label, active-controlled, non-inferiority clinical trial (the ASPIRE-LD trial) conducted in China. It aims to compare the efficacy and safety of low-dose aspirin (50 mg once daily) versus standard-dose aspirin (100 mg once daily), both in combination with a P2Y12 inhibitor, in patients who have successfully undergone percutaneous coronary intervention (PCI) and plan to receive at least 12 months of dual antiplatelet therapy (DAPT). A total of 2640 eligible patients will be randomly assigned in a 1:1 ratio to receive either 50 mg or 100 mg of enteric-coated aspirin daily, plus a P2Y12 inhibitor (ticagrelor 90 mg twice daily or clopidogrel 75 mg once daily, prescribed according to routine clinical practice). All participants will be followed for 12 months after randomization. The primary goal is to verify that 50 mg aspirin is non-inferior to the 100 mg standard dose in preventing major adverse cardiac and cerebrovascular events (MACCE: cardiovascular death, non-fatal myocardial infarction, definite/probable stent thrombosis, and ischemic stroke) at 12 months post-PCI. If non-inferiority is confirmed, the study will further test whether 50 mg aspirin reduces clinically relevant bleeding events (BARC type 2, 3, or 5) better than the standard dose. The study is sponsored by the First Hospital of Jilin University and will be carried out in 10-15 tertiary hospitals across China. Its findings will provide evidence for optimizing aspirin dosing in post-PCI DAPT.

Timeline

Start
2026-03-01
Primary completion
2029-03-01
Completion
2029-04-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Aspirin Small molecule 50 mg Oral
Subject Aspirin Small molecule 100 mg Oral
Background Clopidogrel Small molecule 75 mg —
Background Ticagrelor Small molecule 90 mg —