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NCT06611579NARecruiting

Clinical Study of the inQB8 TTVR System (The MonarQ Study)

inQB8 Medical Technologies, LLC

Start Date

6/1/2025

Completion Date

10/31/2030

Summary

Prospective, multi-center study to assess safety and performance of the inQB8 MonarQ Tricuspid Valve Replacement System.

Detailed Description

The study is a multi-center, prospective, single-arm study to assess safety and performance of the inQB8 Medical Technologies MonarQ Tricuspid Valve Replacement System.

Eligibility Criteria

Age Range: 18 years to No maximum

Inclusion Criteria: * Anatomically suitable for the MonarQ TTVR System * Symptomatic, tricuspid regurgitation (TR) that is severe or greater * Adequately treated for heart failure based upon medical standards * Hemodynamically stable Exclusion Criteria: * Need for emergent or urgent surgery for any reason, any planned cardiac surgery within the next 12 months (365 days), or any planned percutaneous cardiac procedure within the next 90 days * Refractory Heart Failure (HF) that requires or required advanced intervention * Any condition, in the opinion of the investigator, making it unlikely the patient will be able to complete all protocol procedures and follow-up. * Currently participating in another investigational biologic, drug or device study

Interventions

DEVICE

Transcatheter Tricuspid Valve Replacement

Interested in This Trial?

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Conditions

Tricuspid Valve Regurgitation

Locations

Cedars-Sinai Medical Center

Los Angeles, California 90048

United States

Los Robles Hosptial and Medical Center

Thousand Oaks, California 91360

United States

Piedmont Atlanta Hospital

Atlanta, Georgia 30309

United States

North Shore University Hospital

Manhasset, New York 11030

United States

Penn Presbyterian Medical Center

Philadelphia, Pennsylvania 19104

United States

Baylor Heart Hospital

Plano, Texas 75093

United States

AZ Sint-Jan Brugge AV

Bruges, 8000

Belgium

St. Michael's Hospital

Toronto, Ontario M5B1W8

Canada