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Safety and Feasibility of the Transcatheter Tricuspid Valve Repair System (Trialign)

Tricuspid Regurgitation Clinical Trial

Official title:
Safety and Feasibility of the Transcatheter Tricuspid Valve Repair System (Trialign) for the Treatment or Reduction of Moderate to Severe Functional Tricuspid Regurgitation

Clinical Trial Summary

The purpose of the study is to demonstrate safety and feasibility of the transcatheter tricuspid valve repair system (Trialign) for the treatment or reduction of moderate to severe functional tricuspid regurgitation.

Clinical Trial Description

This study is a prospective single-arm trial for transcatheter tricuspid valve repair system (Trialign). A series of physical, imaging and laboratory exams will be performed to determine whether a subject has moderate to severe tricuspid regurgitation with high surgical risk. Subjects who meet the criteria will then receiveTrialign treatment if an informed consent is obtained. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04936802
Study type Interventional
Source Xijing Hospital
Contact Bo Wang
Phone 86-18092798759
Email trialign@163.com
Status Not yet recruiting
Phase N/A
Start date June 25, 2021
Completion date June 30, 2023
View Details
See also
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