MATTERS II - Mistral Percutaneous Tricuspid Valve Repair FIM Study
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Tricuspid Valve Regurgitation
- Sponsor
- Mitralix
- Enrollment
- 9
- Locations
- 4
- Primary Endpoint
- Acute safety, Rate of device related SAE
- Status
- Completed
- Last Updated
- 2 years ago
Overview
Brief Summary
The Mistral is an investigational device intended for percutaneous trans-catheter repair in high risk for surgery individuals suffering from functional Tricuspid Regurgitation (TR).
The device system is to be used only in accordance with the approved Investigational Plan on subjects who have signed an informed consent form. Device use is limited to the approved study investigators.
Detailed Description
The study is designed to clinically demonstrate device acute safety and technical performance (Primary Endpoints) along with longer FU device safety and effectiveness evaluation (Secondary Endpoint). The main objectives of the study are: * Evaluate the Acute safety of the implanted Mistral device post procedure and at 30 day follow up period. * Evaluate the long term Safety of the device. * Demonstrate effectiveness of the Mistral device in reducing TR. Primary endpoints: * Safety: Acute safety. Rate of all SAEs including device related SAEs, all caused mortality, stroke, MI, cardiac tamponade, surgery for failed percutaneous repair and non-elective cardiovascular surgery to treat an adverse event. At discharge and 30 days. * Performance: Mistral Implantation rate of technical success (defined as successful device implantation with grasped chords from at least two leaflets.). Secondary endpoints: * Safety: Safety at 3,6, 12 and 24 months. Rate of all SAEs including device related SAEs at 3, 6, 12 and 24 months. * Effectiveness: TR reduction post-procedure, at discharge and 30 days, 3,6, 12 and 24 months. Improved NYHA class, 6MWTdistance and KCCQ (quality of life) at 30 days, 3,6, 12 and 24 months.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Subject has given signed study Informed Consent for participation prior to procedure.
- •Subject is ≥ 18 years of age or legal age in host country
- •Subject is willing and able to comply with all required follow-up evaluations
- •Genders eligible for the study: Both genders
- •Chronic functional tricuspid regurgitation (FTR) with a minimum of moderate tricuspid regurgitation;
- •o Subjects with moderate TR: Only NYHA Class III or IV maybe considered for inclusion.
- •Subjects with severe or greater TR: NYHA II, III, or IV may be considered for inclusion Subject has left ventricular ejection fraction (LVEF) \>20 %
- •Subject is of functional class 2 or more (NYHA)
- •The subject is high risk to undergo TV surgery as assessed and consented by a cardiac surgeon and an interventional cardiologist at the site (center heart team), and according to ESC/EACTS guidelines on the management of valvular heart disease.
- •Patients with Jugular and/or Femoral veins enabling catheterization with 12Fr catheters
Exclusion Criteria
- •Tricuspid Stenosis \>mild
- •Tricuspid Subvalvular calcification or calcification of the chordae.
- •Subjects with Aortic and/or Mitral valve severe stenosis and/or severe regurgitation.
- •Subjects with severe, uncontrolled hypertension.
- •Subjects with previous tricuspid repair or replacement.
- •Subjects, which need to undergo an emergency surgery.
- •Subjects participating in another clinical investigation.
- •Subject has a history of a cerebral vascular accident (CVA) or transient ischemic attack (TIA) within the past 90 days.
- •Subject has a history of a myocardial infarction (MI) in the past 90 days.
- •Subject has had a percutaneous interventional, including coronary intervention (PCI), within the last 90 days before procedure.
Outcomes
Primary Outcomes
Acute safety, Rate of device related SAE
Time Frame: Until hospital discharge - up to 5 days post procedure day
including device related mortality, stroke, MI, cardiac tamponade, surgery for failed percutaneous repair and non-elective cardiovascular surgery to treat an adverse event.
Acute safety: Rate of device related SAE
Time Frame: At 30 days post procedure
including device related mortality, stroke, MI, cardiac tamponade, surgery for failed percutaneous repair and non-elective cardiovascular surgery to treat an adverse event.
Performance: Mistral Implantation rate of technical success
Time Frame: Procedure
defined as successful device implantation with grasped chords from at least two leaflets.
Secondary Outcomes
- Effectiveness NYHA class(At 24 months post procedure)
- Effectiveness TR(At 24 months post procedure)
- Effectiveness 6MWT(At 24 months post procedure)
- Effectiveness KCCQ(At 24 months post procedure)
- Safety: Rate of all SAEs(At 24 months post procedure)