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Clinical Trial Summary

The study aimed to evaluate the efficacy and safety of transcatheter aortic valve replacement (TAVR) in patients with severe native valve aortic insufficiency. It is a multicentre, observational cohort study. The primary endpoint consisted of a composite of all-cause death, disabling stroke, or rehospitalization for heart failure at 12 months postoperatively. According to previous research results and opinions of expert groups, the sample size was expected to be 76 cases.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05737264
Study type Observational
Source Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
Contact ruqiong nie
Phone +86 13600479016
Email nieruqiong@126.com
Status Recruiting
Phase
Start date December 1, 2022
Completion date October 2023

See also
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