Patients are searching for this trial right now

This page is already ranking on Google. Activate it to start receiving pre-qualified patient leads directly in your inbox.

14-day free trial · $44/mo after · Cancel anytime · Money-back guarantee

NCT07130994 · InnovHeart

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

(CASSINI-US)

What this study is about

CASSINI-US is a forward-looking, single-treatment group$1, conducted at multiple hospitals early feasibility study enrolling up to 15 patients at up to 5 sites in the United States (US).

View original scientific description

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.

Interventions

DEVICE

Mitral Valve Replacement

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

Primary outcome measures

Technical (Implant) Success Endpoint

Time frame: At completion of study procedure (Day 0)

Presented as the n/N (%) of patients that meet the definition of Implant Success per protocol.

Freedom from Major Adverse Events Endpoint

Time frame: 30 days from index procedure

Freedom from (n/N, %) device-related or procedure-related major adverse events (MAE) which include: Cardiovascular death, Peri-procedural myocardial infarction, Disabling stroke, Major cardiac structural complication, Major vascular complication, and Mitral reintervention (operative or transcatheter) due to progressive or recurrent MR or device-related complications.

Mitral Valve Effectiveness Endpoint (reduction in MR grade)

Time frame: 30 days post treatment

Defined as the reduction of mitral regurgitation Grade to ≤1+ at 30 days.

Who can participate

This study lists these criteria on ClinicalTrials.gov. A study coordinator reviews eligibility during screening — this page does not determine whether you qualify.

Inclusion criteria

  • Age 18 years or older.
  • Symptomatic, moderate to severe or severe, functional or mixed, mitral regurgitation (≥ Grade 3+).
  • NYHA functional Class ≥ II. If Class IV, patient must be ambulatory.
  • Ability to tolerate oral anticoagulation.
  • Ability to qualify for bailout surgery (which may include open heart surgery).
  • High risk for open-heart mitral valve surgery due to age, co-morbidities or frailty, as determined by the Heart Team.
  • Willing and able to complete study-related assessments and questionnaires.

Exclusion criteria

  • Purely degenerative (organic/primary) (i.e. intrinsic valve lesions) mitral regurgitation.
  • Excessive frailty or comorbid conditions that preclude the anticipated benefit of the mitral valve replacement.
  • Life expectancy \<1 yr. due to noncardiac conditions.
  • Endocarditis in the 3 months prior to procedure date.
  • Current admission with acute heart failure exacerbation.
  • Dependency on inotropic agents or mechanical circulatory support.
  • Untreated clinically significant CAD.
  • Active systemic infection.
  • Modified Rankin Scale ≥4 disability.
  • Chronic renal failure defined as eGFR \< 30 mL/min/m2 or on renal replacement therapy.
  • Severe pulmonary arterial hypertension (PAH), defined as PASP \> 70mmHg.
  • Platelets \< 90,000.
  • COPD on home oxygen therapy deemed too high risk for intubation.
  • Refuses blood transfusions.
  • Documented bleeding or coagulation disorders (hypo- or hyper-coagulable states).
  • Severe connective tissue disease under chronic immunosuppressive or cortisone therapy.
  • Participating in other investigational studies likely to confound the results or affect the study.
  • Unable or does not sign the study informed consent form.
  • Patients classified as "vulnerable patients" Cardiovascular Exclusion Criteria
  • Myocardial infarction during prior 30 days.
  • Stroke or TIA during prior 90 days.
  • Severe extracardiac arteriopathy (safety measure for extra-circulatory support if surgical conversion is needed).
  • Prior mitral valve treatment (e.g., valve repair or replacement, MitraClip, etc.), and/or anticipated mitral valve treatment prior to enrollment.
  • Prior surgical mechanical valve AVR.
  • Prior TAVI. -Need for any planned cardiovascular surgery or intervention (other than for MV disease) within 30 days post-index procedure.
  • CRT, CRT-D, IPG or ICD implanted in previous 30 days.
  • Cardiogenic shock, hemodynamic instability, Systolic Blood Pressure \<90mmHg, Inotropic dependent or IABP/mechanical circulatory support. CABG or PCI within previous 30 days.
  • Inadequately treated for cardiac condition per applicable standards, such as for coronary artery disease, left ventricular dysfunction, mitral regurgitation, or heart failure, as reviewed by the Patient Screening Committee.
  • Prior or planned heart transplantation (UNOS status 1).
  • Physical evidence of right-sided CHF:
  • Patients with ascites.
  • Patients with anasarca (generalized edema / hydropsy).
  • Hypertrophic cardiomyopathy, restrictive cardiomyopathy, constrictive pericarditis, or other structural heart disease causing heart failure with the exception of dilated ischemic or non-ischemic cardiomyopathy. Procedural Exclusion Criteria
  • Known hypersensitivity or contraindication to procedural or post-procedural medication (e.g., contrast solution, anticoagulation therapy).
  • Documented hypersensitivity to nickel or titanium. Cardiac Imaging Exclusion Criteria (evaluated by Core Labs)
  • Contraindications to TEE imaging
  • Left ventricular EF ≤ 30% by echocardiogram.
  • Severe mitral annular calcification, severe mitral stenosis, valvular vegetation or mass.
  • Extensive mitral flail leaflets
  • Evidence of new or untreated intracardiac thrombus, mass, or vegetation.
  • Severe right ventricular dysfunction.
  • Severe tricuspid regurgitation.
  • Hemodynamically significant inter-atrial shunt (ASD).
  • Severe aortic regurgitation or aortic stenosis.
  • Anatomic ineligibility for SATURN Valve or SATURN TS procedure as determined by the Screening Committee.

Where

  • Los Angeles, California
  • Sacramento, California
  • Thousand Oaks, California
  • New York, New York
  • Portland, Oregon

Collaborators

Avania

Related conditions & keywords

Mitral RegurgitationHeart DiseaseTranscatheterMitral ValveReplacement

Frequently asked questions

What is a clinical trial?

A clinical trial is a research study that tests new medical treatments, drugs, devices, or procedures to determine their safety and effectiveness. Trials are carefully designed and monitored to protect participants while advancing medical knowledge.

Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. Trials must be reviewed and approved, and participants are closely monitored by medical professionals throughout the study. You can withdraw at any time if you choose.

Will I be compensated?

Many clinical trials offer compensation for your time, travel expenses, and inconvenience. The specific compensation varies by study and will be discussed during the screening process. All study-related medical care is typically provided at no cost to participants.

Will I receive a placebo instead of treatment?

When effective treatment exists, participants typically receive either the standard treatment plus the study intervention, or the standard treatment plus placebo. You would not be denied effective care. Placebos are primarily used when no proven treatment is available, or in addition to standard care. Your trial consent form will clearly explain what treatments you may receive.

Can I leave a trial if I change my mind?

Absolutely. Participation in clinical trials is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty or loss of benefits to which you are otherwise entitled.

How long does a clinical trial last?

Trial duration varies widely depending on the study design and purpose. Some trials last just a few weeks, while others may continue for months or years. The study coordinator will provide specific timeline information during your screening call.

Data: ClinicalTrials.gov · synced Aug 10, 2026 · Source of record for eligibility and locations

📊
1 of 15 participants interested
7% interest

See if this study fits

A short prescreen based on this study's listed criteria. A coordinator confirms eligibility — this is not a medical assessment.

Preparing your pre-screening questions…

Study locations

Choose your preferred location, or select flexible during enrollment.

NOT_YET_RECRUITING

Los Angeles

California

Location available
NOT_YET_RECRUITING

Sacramento

California

Location available
RECRUITING

Thousand Oaks

California

Location available
RECRUITING

New York

New York

Location available
NOT_YET_RECRUITING

Portland

Oregon

Location available

Express your interest

Share your contact details and a study coordinator can follow up about screening.

Secure & Confidential

Your information is protected and will only be shared with the research team.

What participation can include

  • Study-related care provided by the research team
  • Close monitoring by medical professionals
  • Possible compensation for time and travel*
  • The option to withdraw at any time
  • Contributing to medical research that may help future patients

*Compensation varies by study. Confirm details with coordinator.

Typical next steps

  1. 1.Submit this form
  2. 2.Phone screening
  3. 3.In-person assessment if eligible
  4. 4.Begin participation

Find More Heart Attack Trials by City

Browse all heart attack clinical trials in these cities — not just this study.

Looking for Mitral Regurgitation Treatment in Los Angeles?

Join others in California exploring innovative treatment options through clinical research

Mitral Regurgitation Treatment Options in Los Angeles, California

If you're searching for Mitral Regurgitation treatment in Los Angeles, participating in a clinical research study may provide access to innovative approaches under expert medical supervision. This study is actively recruiting participants in Los Angeles, Sacramento, Thousand Oaks and surrounding areas.

Clinical trials offer participants the opportunity to receive cutting-edge treatments while contributing to medical research that may help future patients with Mitral Regurgitation. All study-related care is provided at no cost to participants.

Local Sites
3 locations in California
Now Enrolling
Up to 15 participants
Quick Start
Screening available now

Why Consider a Clinical Trial for Mitral Regurgitation?

Potential Benefits

  • Access to new treatment approaches before public availability
  • Close monitoring by experienced medical professionals
  • Study-related care provided at no cost
  • Contribute to medical research for Mitral Regurgitation

What to Expect

  • Initial screening to determine eligibility
  • Regular check-ups and monitoring visits
  • Possible compensation for time and travel
  • You can withdraw at any time

Frequently Asked Questions About This Mitral Regurgitation Study

Important Clinical Trial Information

This information is provided for educational purposes and does not constitute medical advice. Clinical trial participation involves potential risks and benefits. Eligibility requirements apply and will be assessed during the screening process.

Study identifier: NCT07130994. For complete study details, visit ClinicalTrials.gov. Always consult with your healthcare provider before making decisions about your medical care or participating in clinical research.