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).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
330
percutaneous mitral valve repair Percutaneous MitraClip Device Implantation
mitral valve repair or mitral valve remplacement
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
...and 21 more locations
All-cause mortality, unplanned hospitalizations for heart failure and mitral valve reintervention
comparison between arms of: * number and reason of death * number and reason unplanned rehospitalisation for cardiovascular reasons, * number of mitral valve reintervention
Time frame: 12 months
occurrence of a major adverse event
all-cause death, need for non-elective cardiovascular or thoracic surgery, device or procedure-related adverse events, major bleeding complications or serious bleeding, major access site vascular complications, major cardiac structural complications, pulmonary complications (device or procedure-related), stroke and other cerebrovascular events, myocardial infarction, acute kidney injury or progression of chronic kidney disease, arrhythmias and conduction system disturbances, unplanned mitral valve surgery due to device/procedure failure or malfunction, requirement for valve replacement after valve repair failure, unplanned cardiac surgery for any cause
Time frame: 30 days
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