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

Last updated: January 24, 2025
Sponsor: Nantes University Hospital
Overall Status: Active - Recruiting

Phase

N/A

Condition

Congestive Heart Failure

Mitral Valve Regurgitation

Treatment

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

cardiac surgery

Clinical Study ID

NCT03271762
RC17_0002
  • Ages > 18
  • All Genders

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 Criteria

Inclusion

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

  • 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)

Study Design

Total Participants: 330
Treatment Group(s): 2
Primary Treatment: percutaneous mitral valve repair with MITRACLIP NT, MITRACLIP NTR/XTR, MITRACLIP G4NT/XT, MITRACLIP G4NTW/XTW
Phase:
Study Start date:
March 02, 2018
Estimated Completion Date:
May 31, 2028

Connect with a study center

  • Chu Angers

    Angers,
    France

    Active - Recruiting

  • Ch Annecy

    Annecy, 74370
    France

    Active - Recruiting

  • Chu Bordeaux

    Bordeaux,
    France

    Active - Recruiting

  • Clinique Saint Augustin

    Bordeaux, 33000
    France

    Site Not Available

  • Chru Brest

    Brest,
    France

    Active - Recruiting

  • Hopital Henri Mondor Aphp

    Créteil,
    France

    Active - Recruiting

  • Chu Grenoble

    Grenoble,
    France

    Active - Recruiting

  • Centre Chirurgical Marie Lannelongue

    Le Plessis-Robinson,
    France

    Active - Recruiting

  • Chru Lille

    Lille, 59000
    France

    Active - Recruiting

  • Hopital Prive Le Bois Lille

    Lille, 59000
    France

    Active - Recruiting

  • CHU LYON

    Lyon,
    France

    Active - Recruiting

  • Clinique de La Sauvegarde

    Lyon, 69009
    France

    Active - Recruiting

  • Hopital La Timone

    Marseille,
    France

    Site Not Available

  • Hopital Prive Clairval

    Marseille, 13009
    France

    Site Not Available

  • Hopital St Joseph

    Marseille,
    France

    Site Not Available

  • Institut Hospitalier Jacques Cartier

    Massy,
    France

    Active - Recruiting

  • Clinique Du Millenaire

    Montpellier, 34000
    France

    Active - Recruiting

  • Chu Nantes

    Nantes,
    France

    Active - Recruiting

  • Hopital Bichat

    Paris,
    France

    Active - Recruiting

  • Hopital Europeen Georges Pompidou

    Paris,
    France

    Active - Recruiting

  • Hopital La Pitie Salpetriere

    Paris,
    France

    Active - Recruiting

  • Institut Mutualiste Montsouris

    Paris,
    France

    Active - Recruiting

  • Chu Poitiers

    Poitiers,
    France

    Active - Recruiting

  • Chu Rennes

    Rennes,
    France

    Active - Recruiting

  • CHU de Rouen

    Rouen,
    France

    Active - Recruiting

  • CHU Félix Guyon

    Saint-Denis, 97400
    France

    Active - Recruiting

  • Centre Cardiologique Du Nord

    Saint-Denis,
    France

    Active - Recruiting

  • Chu Saint Etienne

    Saint-Étienne, 42277
    France

    Active - Recruiting

  • Hopital Civil Strasbourg

    Strasbourg,
    France

    Active - Recruiting

  • Clinique Pasteur

    Toulouse,
    France

    Active - Recruiting

  • Hopital Rangueil

    Toulouse,
    France

    Active - Recruiting

  • Chru Tours

    Tours,
    France

    Active - Recruiting

  • Clinique Du Tonkin

    Villeurbanne, 69100
    France

    Active - Recruiting

  • Centre Cardio-Thoracique de Monaco

    Monaco,
    Monaco

    Site Not Available

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