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Clinical Trial Summary

To evaluate the efficacy of drug-coated balloon versus drug-eluting stent for the treatment of large de novo coronary lesions(RVD=2.75~4.0mm).


Clinical Trial Description

Patients were randomly assigned (1:1) to receive angioplasty with DCB or implantation of a DES. Dual anti-platelet therapy was given according to current guidelines. Follow-up was originally scheduled at by telephone or clinical visit at 1 month, 6 months, and 12 months after discharge. The primary endpoint is a composite endpoint of cardiac death, target vessel related myocardial infarction, and target lesion revascularization (TLF) at 12 months follow up. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05101005
Study type Interventional
Source Lepu Medical Technology (Beijing) Co., Ltd.
Contact Yansong Li
Phone 8618221277176
Email liyansong021@126.com
Status Not yet recruiting
Phase N/A
Start date October 2021
Completion date November 2023

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