Ireland
--:--IST
Active, not recruiting Not applicable

Multicentre Study of MITRACLIP® Transcatheter Mitral Valve Repair in Patients With Severe Primary Mitral Regurgitation Eligible for High-risk Surgery

NCT03271762 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2018-03-02
Last updated
2025-11-26

Condition(s) studied

Mitral Regurgitation

Investigational drug(s) / intervention(s)

percutaneous mitral valve repair with MITRACLIP NT, MITRACLIP NTR/XTR, MITRACLIP G4NT/XT, MITRACLIP G4NTW/XTWcardiac surgery

percutaneous mitral valve repair with MITRACLIP NT, MITRACLIP NTR/XTR, MITRACLIP G4NT/XT, MITRACLIP G4NTW/XTW: percutaneous mitral valve repair Percutaneous MitraClip Device Implantation

cardiac surgery: mitral valve repair or mitral valve remplacement

Study summary

The objective of the study is to demonstrate the non-inferiority for clinical efficacy of an endovascular treatment strategy with the MitraClip® in comparison with a surgical treatment strategy in patients with severe primary mitral regurgitation judged eligible for anatomical repair with the MitraClip® or mitral valve surgery with high surgical risk.

This trial is a French and Monegasque, multicenter and randomized trial. Patients enrolled will be clinically followed for 2 years ( clinical visit at 1 month, at 6 months and 12 months, phone call at 18 months and clincial visit at 24 months).

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: Primary Mitral Regurgitation grade 3+ or 4+ * Patients in class II to IV NYHA * Mitral valve anatomy appropriate to MitraClip® therapy and mitral valve surgery * Adult patients judged eligible for mitral valve surgery by the local heart team but at high surgical risk defined as: age ≥ 75 years and STS score ≥ 6 % or one frailty index or one major organ system compromise or one possible procedure-specific impediment (using MVARC definitions) ; or age \< 75 years and STS score \> 8 % or at least one other high-risk criterion following the MVARC definitions; or age \> 80 years and judged at high risk for surgery by the local heart team * Isolated Mitral valve pathology * If revascularization procedures are required, they must be performed more than 30 days from intervention (D0) * Patients affiliate to social security Non-inclusion Criteria: * Life expectancy \< 1 year due to non-cardiac conditions * Secondary Mitral regurgitation * Evolving endocarditis or active endocarditis or inflammatory disease in the last 3 months * Patient who cannot tolerate procedural anticoagulation or post procedural antiplatelet regimen * Rheumatic mitral valve disease * Evidence of intracardiac, inferior vena cava or femoral venous thrombus * Valve anatomy not compatible with MitraClip® implantation (cf. colum 3 table 3 page 57) * Stroke or transient ischaemic event within 30 days before D0 * Modified Rankin Scale ≥4 disability (appendix 9) * TAVR within 30 days before D0-Untreated, clinically significant coronary artery disease requiring revascularization * Any percutaneous cardiovascular intervention within 30 days before D0 including ATC * Cardiovascular surgery, or carotid surgery within 30 days before D0 * Any prior mitral valve surgery or transcatheter mitral valve procedure * Need for any concomitant cardiac surgery including treatment of severe secondary tricuspid regurgitation in accordance with class I recommendation in 2017 ESC guidelines. Surgical treatment of mild or moderate secondary tricuspid regurgitation (Class IIa and IIb recommendations) can still be performed in the protocol according to the local heart team decison * NYHA functional class I * LVEF \< 30% * Primary MR grade 1 to 2 * Subjects in whom transesophageal echocardiography or transseptal catheterization are contraindicated or high-risk * Any condition preventing the patient from completing all protocol procedures (including compliance with guidelines directed medical therapy) and follow-up visits * Patient unable or unwilling to provide written, informed consent before study enrolment * Pregnant or nursing women * Vulnerable people: persons deprived of liberty; under trusteeship or under curatorship * Participation in another trial that would interfere with this trial Exclusion criteria * Not eligible for a MitraClip® intervention after Core Lab evaluation * Before randomization (D-21) the patient no longer fulfills eligibility criteria (inclusion criteria and non-inclusion criteria)

Primary outcome measure(s)

  • All-cause mortality, unplanned hospitalizations for heart failure and mitral valve reintervention — 12 months
    comparison between arms of: * number and reason of death * number and reason unplanned rehospitalisation for cardiovascular reasons, * number of mitral valve reintervention

Trial sites (31)

FacilityCityRegionStatus
Chu Angers Angers France
Ch Annecy Annecy France
Chu Bordeaux Bordeaux France
Chru Brest Brest France
Hopital Henri Mondor Aphp Créteil France
Chu Grenoble Grenoble France
Centre Chirurgical Marie Lannelongue Le Plessis-Robinson France
Chru Lille Lille France
Hopital Prive Le Bois Lille Lille France
Clinique de La Sauvegarde Lyon France
CHU LYON Lyon France
Hopital La Timone Marseille France
Hopital St Joseph Marseille France
Institut Hospitalier Jacques Cartier Massy France
Clinique Du Millenaire Montpellier France
Chu Nantes Nantes France
Hopital Bichat Paris France
Hopital Europeen Georges Pompidou Paris France
Hopital La Pitie Salpetriere Paris France
Institut Mutualiste Montsouris Paris France
Chu Poitiers Poitiers France
Chu Rennes Rennes France
CHU de Rouen Rouen France
CHU Félix Guyon Saint-Denis France
Centre Cardiologique Du Nord Saint-Denis France
Chu Saint Etienne Saint-Etienne France
Hopital Civil Strasbourg Strasbourg France
Clinique Pasteur Toulouse France
Hopital Rangueil Toulouse France
Chru Tours Tours France
Clinique Du Tonkin Villeurbanne France
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT03271762 on ClinicalTrials.gov ↗ ← All trials in France