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Clinical Trial Summary

The purpose is to evaluate the safety, effectiveness and performance of Venus-Vitae Transcatheter Heart Valve System in patients with severe aortic stenosis.


Clinical Trial Description

This trial is a prospective, multi-center, non-randomized interventional study to evaluate the safety, effectiveness and performance of the Venus-Vitae Transcatheter Heart Valve System in patients with severe aortic stenosis. Clinical visits will be scheduled at screening, pre-discharge, 30 days, 6 months, 12 months and annually thereafter to 5 years. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05991271
Study type Interventional
Source Venus MedTech (HangZhou) Inc.
Contact
Status Not yet recruiting
Phase N/A
Start date October 31, 2023
Completion date June 30, 2029

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