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Clinical Trial Summary

This study is a multicenter, randomized, controlled clinical research and aims to evaluate the safety and efficacy of the paclitaxel drug-coated coronary artery balloon catheter in patients with coronary artery in-stent restenosis compared to seQuent® please paclitaxel drug-coated coronary artery balloon catheter.


Clinical Trial Description

This prospective, multicenter, randomized controlled clinical study is designed to enroll 216 subjects with in-stent restenosis and randomly assign them to the trial and control groups on a 1:1 basis.The experimental group was treated with paclitaxel drug-coated coronary artery balloon catheter, and the control group was treated with SeQuent ® Please paclitaxel balloon catheter, which has been marketed. In-segment late lumen loss 9 months after surgery was the main end point of the study. All subjects were followed up clinically at 1 month, 6 months, 9 months, 1 year and 2 years after the surgery, and were followed up with angiography at 9 months after the surgery. ;


Study Design


Related Conditions & MeSH terms

  • Coronary Artery In-stent Restenosis

NCT number NCT04386213
Study type Interventional
Source Shanghai MicroPort Medical (Group) Co., Ltd.
Contact Ling Tao
Phone 13636498543
Email clfeng@microport.com
Status Not yet recruiting
Phase N/A
Start date September 1, 2020
Completion date July 31, 2025