Optimal antiPlatelet Therapy for High Bleeding and Ischemic RISK Patients Trial (OPT-BIRISK)

Shenyang Northern Hospital

Status and phase: Completed; Phase 4

Conditions: Prolonged DAPT in ACS Patients With Hisk of Both Ischemic and Hemorrhage

Treatments: Drug: Clopidogrel; Drug: Clopidogrel+aspirin

Study type: Interventional

Funder types: Other

Identifiers

NCT03431142

CLOPIL08732

Details and patient eligibility

About

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.

Full description

Current guidelines recommend that patients with ACS undergoing stent implantation might be offered extended DAPT treatment for up to 30 months if necessary. For patients with high risk of both ischemic and hemorrhage, despite prolonged use of DAPT may bring antithrombotic benefit, it may also increase the risk of bleeding. There is an urgent need for specific guiding on intensive antiplatelet therapy in this population of patients to reduce the risk of ischemia and to avoid the risk of bleeding.

Previous studies have shown that, after 12 months of DAPT treatment, continuation of clopidogrel monotherapy may further reduce the risk of ischemia and bleeding compared with aspirin. 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.

Enrollment: 7,758 patients

Sex: All

Ages: 18 to 85 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• ACS patients undergoing PCI (New-Generation DES) and finishing 9-12 months of DAPT
• 18 ~ 85 years old adult patients
• Patients under the age of 65 must meet at least one of the following clinical criteria of high bleeding risk and at least one of the following clinical criteria of high ischemic risk; Patients aged 65-75 must meet one of the following clinical criteria of either high bleeding risk or high ischemic risk.

Clinical criteria of high bleeding risk:

• ≥75 years old
• female
• Iron deficiency anemia
• history of stroke (hemorrhagic or ischemic)
• ongoing medical treatment of diabetes (oral hypoglycemic agents or subcutaneous insulin)
• Chronic kidney disease (eGFR <60mL/min or creatinine clearance<60mL/min)

Clinical criteria of high ischemic risk:

• ≥75 years old
• Multiple coronary lesions
• target lesions required for stent of total length> 30mm
• Thrombotic target lesions
• Bifurcation lesions are Medina 0, 1, 1 or 1, 1, and 1, with stents implanted in both main branch and side branch
• Left main coronary artery (≥50%) or proximal LAD (≥70%) lesions
• Calcified plaques requiring endovascular excision
• acute coronary syndrome with troponin positive
• Previous myocardial infarction, ischemic stroke, diagnosed peripheral arterial disease (PAD), or revascularization due to coronary artery disease (CAD) / PAD
• recurrent myocardial infarction, revascularization, stent thrombosis, stroke in the last 9 months
• ongoing medical treatment of diabetes (oral hypoglycemic agents or subcutaneous insulin)
• Chronic kidney disease (eGFR<60 mL/min or creatinine clearance <60 mL/min)

Exclusion criteria

• Discontinuation or termination of DAPT treatment during the past 6 months due to adverse events (bleeding or ischemia) or other conditions
• Surgery plan within 90 days
• Coronary Revascularization (Surgical or Intervention) Program within 90 days
• Dialysis-dependent renal failure
• Moderate or severe hepatic insufficiency (2 times the upper limit of normal for ALT or AST)
• Life expectancy <1 year
• Unable or unwilling to provide informed consent
• Women with childbearing potential
• Platelet count <100000/mm3
• Subjects undergoing warfarin or similar anticoagulant therapy

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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7,758 participants in 2 patient groups

Clopidogrel monotherapy

Experimental group

Description:

On the basis of 9-12 months of DAPT(aspirin+clopidogrel), continue clopidogrel monotherapy in the following 9 months.

Treatment:

Drug: Clopidogrel

Clopidogrel plus aspirin

Active Comparator group

Description:

On the basis of 9-12 months of DAPT(aspirin+clopidogrel), continue DAPT (aspirin+clopidogrel) in the following 9 months.

Treatment:

Drug: Clopidogrel+aspirin