Suture-mediated Closure System Following Endovascular Peripheral Arterial Procedures

Percutaneous Intervention Via Femoral Artery Clinical Trial

Official title: Prospective, Multi-center, Randomized Controlled Study to Evaluate the Effectiveness and Safety of Suture-mediated Closure System Following Endovascular Peripheral Arterial Procedures

Status Not yet recruiting

Clinical Trial Summary

The purpose of this study is to evaluate the effectiveness and safety of the suture-mediated closure system produced by Suzhou Hengrui Hongyuan Medical Technology Co., Ltd. following endovascular peripheral arterial procedures.

Clinical Trial Description

Prospective, multi-center, randomized Comparative study using the Suture-mediated Closure System produced by Suzhou Hengrui Hongyuan Medical Technology Co., Ltd.as an investigational device and the Perclose® ProGlide Suture-Mediated Closure System as a comparator.

After going through the confirmation of inclusion/exclusion criteria with signed subjects, they will have a procedure either of the two devices. The subjects should follow designated physician's instructions accurately during the clinical trial period. There are about 4 times evaluations Including screening. ;

Related Conditions & MeSH terms

• Percutaneous Intervention Via Femoral Artery

• NCT number: NCT05899478
• Study type: Interventional
• Source: Suzhou Hengruihongyuan Medical Technology Co. LTD
• Status: Not yet recruiting
• Phase: N/A
• Start date: June 2023
• Completion date: May 2024