Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07414342

Safety and Efficacy of the RENATUS® Transcatheter Aortic Valve System for the Treatment of Severe Aortic Stenosis

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
800 (estimated)
Sponsor
Beijing Balance Medical Technology Co., Ltd · Industry
Sex
All
Age
60 Years – 100 Years
Healthy volunteers
Not accepted

Summary

This study is a prospective, non-randomized, observational, post-market follow-up trial designed to evaluate the safety and efficacy of the RENATUS® Transcatheter Aortic Valve System for the treatment of severe aortic stenosis.

Conditions

Interventions

TypeNameDescription
DEVICERENATUS® TAVRRENATUS® Transcatheter Aortic Valve System,an approved marketed TAVR

Timeline

Start date
2026-02-01
Primary completion
2027-09-01
Completion
2037-09-01
First posted
2026-02-17
Last updated
2026-02-17

Locations

4 sites across 1 country: China

Source: ClinicalTrials.gov record NCT07414342. Inclusion in this directory is not an endorsement.

Safety and Efficacy of the RENATUS® Transcatheter Aortic Valve System for the Treatment of Severe Aortic Stenosis (NCT07414342) · Clinical Trials Directory