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Clinical Trial Summary

The study is aimed to assess the safety and feasibility of the Tioga TMVR System in treating patients with symptomatic MR (MR>=3+)


Clinical Trial Description

The Tioga TMVR Feasibility Study is a prospective, single-arm, multi-center study with a planned enrollment of up to 30 patients. The Tioga TMVR System is designed to percutaneously replace a patient's diseased native mitral valve with a bioprosthetic valve. The investigational device is intended for transseptal replacement of the mitral valve in patients with symptomatic MR (MR>=3+). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06038838
Study type Interventional
Source Tioga Cardiovascular, Inc.
Contact Andrew Fu
Phone (408) 560-2500
Email andrew.fu@tiogamed.com
Status Not yet recruiting
Phase N/A
Start date December 1, 2023
Completion date December 1, 2026

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