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Clinical Trial Summary

This prospective, multicenter, randomized, controlled study is designed to evaluate the safety and effectiveness of the Tri-wire Peripheral Balloon Dilatation Catheter compared to a standard PTA Catheter in treating subjects presenting with clinical and hemodynamic abnormalities in native arteriovenous (AV) fistulae located in the upper extremity.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04393688
Study type Interventional
Source BrosMed Medical Co., Ltd
Contact Qizhuang Jin
Phone 13301011122
Email jinqizhuang@bjmu.edu.cn
Status Not yet recruiting
Phase N/A
Start date May 25, 2020
Completion date May 1, 2021

See also
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