Safety and performance evaluation of the CARLEN System in patients with functional mitral valve regurgitation.
The purpose of this early feasibility study (EFS) is to evaluate the safety and performance of the CARLEN System in patients with symptomatic, moderate-to-severe or severe (MR ≥ 3+), functional (or secondary) mitral regurgitation.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
30
CARLEN System
Primary Endpoint
Freedom from device- or procedure-related serious adverse events through 30-days post-procedure
Time frame: 30-days post-procedure
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.