15 Participants NeededMy employer runs this trial

Mitral Valve Replacement for Mitral Regurgitation

(CASSINI-US Trial)

Recruiting at 5 trial locations
AR
DW
Overseen ByDavid Wilson
Age: 18+
Sex: Any
Trial Phase: Academic
Sponsor: InnovHeart
Must be taking: Anticoagulants
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial tests a new treatment for individuals with moderate to severe mitral regurgitation, a heart condition where the mitral valve fails to close properly, causing blood to flow backward in the heart. The trial evaluates the safety and effectiveness of the SATURN TS TMVR System, a device implanted through a catheter, both immediately after the procedure and over time. Ideal participants are those who experience significant symptoms from mitral regurgitation, can tolerate blood-thinning medication, and face high risks with traditional open-heart surgery. As an unphased trial, this study provides an opportunity to contribute to groundbreaking research and potentially benefit from an innovative treatment.

Do I have to stop taking my current medications for the trial?

The trial information does not specify if you need to stop taking your current medications. However, you must be able to tolerate oral anticoagulation, and there should be no known hypersensitivity or contraindication to procedural or post-procedural medication.

What prior data suggests that the SATURN TS TMVR System is safe for treating mitral regurgitation?

In a previous study with the SATURN TS TMVR System, researchers found that 14% of 50 patients passed away within 30 days. The same study showed a 98% success rate for the procedure, indicating correct device implantation in most cases. Another report noted that the SATURN valve performed well and was safe, with patients showing significant improvements in heart valve function after the procedure. However, these results suggest that while the treatment is promising, some risks remain. Prospective participants should consider these findings when deciding to join a trial.12345

Why are researchers excited about this trial?

Most treatments for mitral regurgitation involve surgical options like open-heart surgery or minimally invasive techniques such as percutaneous edge-to-edge repair. However, the SATURN TS TMVR System is unique because it offers a transseptal approach to mitral valve replacement, which is less invasive than traditional surgery. This system allows for valve replacement through a catheter inserted via a small incision, potentially reducing recovery times and surgical risks. Researchers are excited about this treatment because it could provide a safer, more efficient alternative for patients who are high-risk surgical candidates or those who prefer a less invasive procedure.

What evidence suggests that the SATURN TS TMVR System is effective for mitral regurgitation?

Research has shown that the SATURN TS TMVR System may help treat mitral regurgitation, a condition where a heart valve fails to close properly, causing blood to leak backward. Participants in this trial will receive the SATURN TMVR System implant. Early results suggest successful placement of this system in patients, leading to improved health outcomes. In initial human trials, the SATURN valve was implanted with positive results, including fewer symptoms and a stable heart valve. Studies indicate that the system is safe and can be inserted using less invasive techniques. While more information is needed, these findings offer promise for those considering this treatment.12456

Who Is on the Research Team?

TP

Torsten P Vahl, MD

Principal Investigator

Columbia University

Are You a Good Fit for This Trial?

This trial is for adults with moderate to severe mitral valve leakage (mitral regurgitation) who have symptoms and are considered high risk for open-heart surgery. Participants must be able to take blood thinners, walk if in the most severe heart failure class, and complete study assessments.

Inclusion Criteria

I can take blood thinners by mouth without issues.
I have moderate to severe symptoms from mitral valve leakage.
I am 18 years old or older.
See 4 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks
1 visit (in-person)

Baseline (Pre-procedure)

Baseline assessments including physical examination, vital signs, and laboratory testing

1 day
1 visit (in-person)

Intraprocedural

Implantation of the SATURN TMVR System and immediate post-procedure assessments

1 day
1 visit (in-person)

Post-procedure Monitoring

Monitoring for acute safety and performance of the implant

7 days
2 visits (in-person)

Follow-up

Participants are monitored for safety and effectiveness after treatment

5 years
Multiple visits (in-person) at 1 month, 3 months, 6 months, 1 year, and annually thereafter

What Are the Treatments Tested in This Trial?

Interventions

  • SATURN TS TMVR System

Trial Overview

The study tests a new minimally invasive device called the SATURN TMVR System that replaces the faulty mitral valve using a catheter instead of open-heart surgery. All participants receive this treatment at select US hospitals.

How Is the Trial Designed?

1

Treatment groups

Experimental Treatment

Group I: SATURN TMVR CohortExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

InnovHeart

Lead Sponsor

Trials
2
Recruited
50+

Avania

Industry Sponsor

Trials
59
Recruited
10,000+

Citations

NCT06414265 | Reduction of Mitral Regurgitation With the ...

The purpose of the study is to evaluate feasibility, safety, and performance of the SATURN TS TMVR System for the treatment of moderate-to-severe or severe, ...

InnovHeart Announces First-In-Human Implantation of ...

In this first clinical use of the low-profile Saturn, the mitral heart valve was successfully implanted transapically in a 72-year-old man with ...

Transseptal Transcatheter Mitral Valve Replacement With a ...

This first reported case of transseptal TMVR with the Saturn valve demonstrates the feasibility and utility of this device. Funding Support and ...

Early Human Experience with the Trans-Septal Saturn ...

The transseptal SATURN system offers a novel solution for MR reduction and annular stabilization. • The SATURN TMVR bioprosthesis has several unique advantages ...

Reduction of Elimination of Mitral Regurgitation With the ...

The purpose of the study is to evaluate the technical (implant) feasibility, and safety, and performance of the SATURN TS TMVR System for the ...

TMVR for the Treatment of Mitral Regurgitation - PMC - NIH

In the first pilot trial (50 patients), the 30-day mortality rate was 14%, with a procedural success rate of 98% and mild or no residual MR ...