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Clinical Trial Summary

This was a prospective, multicenter, randomized, controlled, non-inferiority clinical study with the primary objective of validating the safety and efficacy of the Suture-Mediated Closure System for percutaneous closure of the common femoral artery puncture site.


Clinical Trial Description

This study was a prospective, multicenter, randomized, controlled, non-inferiority clinical trial. It is planned to be conducted in multiple clinical trial institutions and enroll 228 subjects. Eligible subjects were randomly divided into the experimental group or the control group at a ratio of 1:1. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05841836
Study type Interventional
Source Zhejiang Zylox Medical Device Co., Ltd.
Contact Yu Zhao, Master
Phone 13808338199
Email 820994765@qq.com
Status Recruiting
Phase N/A
Start date October 26, 2022
Completion date July 30, 2023

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