Rivaroxaban Combined With DAPT Versus DAPT Alone After Drug-coated Balloon Angioplasty
Acute Coronary Syndrome
About this trial
This is an interventional treatment trial for Acute Coronary Syndrome
Eligibility Criteria
Inclusion Criteria: ACS patients who meet the indications of percutaneous coronary intervention The reference diameter of the target vessel was ≥2.75mm Target lesions were treated with a drug-coated balloon catheter (DCB) for PCI According to IVUS assessment, the target lesions were dissected and accumulated medium without affecting distal blood flow Exclusion Criteria: <18 or >60 years old Bridging vessels or stent restenosis Unable to sign written informed consent Female patients during pregnancy or lactation (for women who have not stopped menstruation, pregnancy test should be performed within 7 days prior to enrollment in this study) Antiplatelet agents and anticoagulants are not available; Have heparin, contrast agent and other allergies The subjects were participating in other uncompleted clinical trials Scheduled elective surgery Life expectancy is less than 1 year Patients with high blood risk Has long-term oral anticoagulant therapy adaptation Cardiogenic shock Patients with severe intraoperative dissection or hematoma requiring stent rescue
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
DAPT+rivaroxaban
DAPT
Rivaroxaban 2.5 mg bid + aspirin 100 mg qd + ticagrelor 90 mg bid was used for 1 month after operation, and then aspirin 100 mg + ticagrelor 90 mg bid was used for 5 months.
aspirin 100 mg qd + ticagrelor 90 mg bid for 6 months.