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Clinical Trial Summary

This is a prospective, multicenter, randomized controlled clinical investigation aiming to evaluate the safety and effectiveness of non-slip balloon catheter for the treatment of patients with coronary artery stenosis.


Clinical Trial Description

This trial is a prospective, multicenter, randomized controlled clinical trial. 200 subjects are expected to be recruited in 7 research centers in China and randomly divided into two groups according to the ratio of test group: control group = 1:1. The primary endpoint is the acute lumen gain. All subjects receive clinical follow-up during hospitalization and 30 days after surgery. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05606367
Study type Interventional
Source Shanghai MicroPort Rhythm MedTech Co., Ltd.
Contact Tingting Wu, M.D.
Phone 0086-021-38954600
Email TingTing.Wu2@microport.com
Status Recruiting
Phase N/A
Start date January 3, 2023
Completion date October 2023

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