drugset / Trial / NCT03431142

Optimal antiPlatelet Therapy for High Bleeding and Ischemic RISK Patients Trial

NCT03431142 ↗

Phase 4 Completed 7758 enrolled Shenyang Northern Hospital
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Current guidelines recommend that patients with ACS undergoing stent implantation might be offered extended DAPT treatment for up to 30 months if necessary. Therefore, we designed a prospective, multicenter, randomized, placebo-controlled trial among ACS patients with high-risk on ischemic and bleeding who received a new generation of DES and received 9 to 12 months of DAPT, and evaluated whether clopidogrel monotherapy reduce the risk of bleeding compared with clopidogrel plus ASA in the following 9 months and achieved non-inferior outcomes in preventing ischemic risk.

Timeline

Start
2018-02-12
Primary completion
2020-12-30
Completion
2020-12-30

Outcome

Met primary endpoint

paper 127 of 3885 patients (3.3%) assigned to clopidogrel plus aspirin (hazard ratio [HR], 0.75; 95% CI, 0.57-0.97; difference, -0.8%; 95% CI, -1.6% to -0.1%; P = .03). PMID 38630489 ↗

Drugs

EvaluationDrugModalityDoseRoute
Comparator Aspirin Small molecule — —
Subject Clopidogrel Small molecule — —

Indications

No indication recorded.