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Clinical Trial Summary

The purpose of the study is to evaluate the safety and performance of the MIA Minimally Invasive Annuloplasty Device in patients with chronic functional tricuspid regurgitation.


Clinical Trial Description

The purpose of the study is to evaluate the safety and performance of the MIA Minimally Invasive Annuloplasty Device in patients with chronic functional tricuspid regurgitation. The study is a prospective, multi-center safety and performance study. Enrolled subjects will be assessed for clinical follow-up at 1 month, 6 months, and 1 year post implant procedure. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03692598
Study type Interventional
Source Micro Interventional Devices
Contact Willard Hennemann, PhD
Phone 215 600-1273
Email bhennemann@microinterventional.com
Status Recruiting
Phase N/A
Start date December 2016
Completion date December 2022

See also
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