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Clinical Trial Summary

A prospective ,Multiple Center Study About the Safety and Efficacy of WeFlow-Tribranch Embedded Aortic Triple-branch Arch Stent Graft System manufactured by EndoNom Medtech (Hangzhou) Co., Ltd. for true/pseudo aortic arch aneurysms and ulcers involving aortic arch . (GENIUS Study)


Clinical Trial Description

This study is a prospective ,multiple center study about the safety and efficacy of WeFlow-Tribranch Embedded Aortic Triple-branch Arch Stent Graft System , it is expected to complete the implantation of 90 patients in 20 centers within 20 months, and interim follow-up was conducted before discharge, 30 days after surgery, 6 months after surgery and 12 months after surgery, long-term follow-up will be performed at 24th month, 36th month, 48th month and 60th month postoperatively. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06385379
Study type Interventional
Source Hangzhou Endonom Medtech Co., Ltd.
Contact Wei Guo
Phone 13910758706
Email Pla301dml@vip.sina.com
Status Recruiting
Phase N/A
Start date June 30, 2024
Completion date December 31, 2030

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