RecruitingNot ApplicableNCT07130994

Reduction or Elimination of Mitral Regurgitation With the SATURN TMVR System (CASSINI-US)

Reduction or Elimination of Mitral Regurgitation With the SATURN Trans-septal TMVR System in Patients With Severe, Symptomatic Mitral Regurgitation (Cassini-US)


Sponsor

InnovHeart

Enrollment

15 participants

Start Date

Aug 5, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

CASSINI-US is a prospective, single-arm, multicenter early feasibility study enrolling up to 15 patients at up to 5 sites in the United States (US). The purpose of the study is to evaluate the technical (implant) feasibility, and safety, and performance of the SATURN TS TMVR System for the treatment of moderate-severe or severe, symptomatic mitral regurgitation through a transcatheter approach. Primary objectives evaluate the implant feasibility, and acute safety and performance of the SATURN TS TMVR System. The secondary objective and additional outcome measures characterize the long-term safety and performance of the SATURN TS TMVR System.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a medical device called Mitral Valve Replacement for people with heart disease and mitral regurgitation. The study is currently recruiting participants at 5 locations.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DEVICEMitral Valve Replacement

Implant of SATURN TS TMVR System for the treatment of moderate-severe or severe, symptomatic mitral regurgitation


Locations(5)

Cedars-Sinai Medical Center

Los Angeles, California, United States

UC Davis Health

Sacramento, California, United States

Los Robles Regional Medical Center

Thousand Oaks, California, United States

Columbia University Irving Medical Center/New York Presbyterian Hospital

New York, New York, United States

Oregon Health & Science University

Portland, Oregon, United States

View Full Details on ClinicalTrials.gov

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NCT07130994


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