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Clinical Trial Summary

To confirm the safety and efficacy of the Lotus™ Valve System in the Chinese population for Transcatheter Aortic Valve Implantation (TAVI) in symptomatic patients with severe aortic stenosis.


Clinical Trial Description

n/a


Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT02536703
Study type Interventional
Source Second Affiliated Hospital, School of Medicine, Zhejiang University
Contact Xianbao Liu, MD
Phone +86-13857173887
Email liuxb2009@hotmail.com
Status Not yet recruiting
Phase Phase 3
Start date September 2015
Completion date December 2020

See also
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