Early Feasibility Study (EFS) of the Nyra Cardiac Leaflet Enhancer (CARLEN) System
a study on Mitral Regurgitation Functional
Summary
- Eligibility
- for people ages 21 years and up (full criteria)
- Location
- at UC Davis
- Dates
- study startedstudy ends around
Description
Summary
Safety and performance evaluation of the CARLEN System in patients with functional mitral valve regurgitation.
Official Title
ENHANCE EFS: Early Feasibility Study (EFS) of the Nyra Cardiac Leaflet Enhancer (CARLEN) System
Details
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.
Keywords
Mitral Regurgitation Functional, CARLEN System
Eligibility
You can join if…
Open to people ages 21 years and up
- Age > 21 years at time of enrollment
- Patient has provided informed consent, is willing and capable of participating in all testing, and agrees to return for all required post-procedure follow-up visits
- Moderate-to-severe or severe (MR ≥ 3+) functional (secondary) mitral valve regurgitation
- Symptomatic with mitral regurgitation (NYHA Class II, III, or ambulatory IV) despite maximally-tolerated guideline-directed medical therapy (GDMT) as determined by the local multidisciplinary Heart Team
- Patient is suitable for transcatheter mitral valve repair as determined by the local multidisciplinary Heart Team and confirmed by the Eligibility Committee
You CAN'T join if...
- Estimated life expectancy of less than 12 months
- Women who are pregnant, lactating, or planning to become pregnant during the clinical study. Women of child-bearing potential must have negative pregnancy test result within 2 weeks prior to the procedure
- Left Ventricular Ejection Fraction (LVEF) < 20%
- Left ventricular end diastolic diameter (LVEDD) > 75 mm
- Acute hemodynamic decompensation
- Known hypersensitivity or contraindications to necessary and routine medications including contrast compounds or components used in the CARLEN System that cannot be successfully pre-medicated, including nitinol, an alloy of nickel and titanium
- Contraindicated for transesophageal echo (TEE)
- Presence of other anatomical characteristics and/or significant comorbidities that in the judgement of the Investigator or Eligibility Committee precludes the subject from participation
- Aortic valve disease requiring intervention or intervention
- Severe or greater tricuspid regurgitation
- Severe right ventricular dysfunction
- Severe pulmonary hypertension
- Presence of significant congenital heart disease
- Planned or scheduled cardiac surgery within next 12 months
- Endocarditis within last 90 days
- Evidence of intracardiac mass, vegetation, or inflammatory or infectious valve disease
Locations
- University of California, Davis
accepting new patients
Sacramento California 95616 United States - The Christ Hospital
accepting new patients
Cincinnati Ohio 45219 United States - University of Michigan
accepting new patients
Ann Arbor Michigan 48109 United States
Details
- Status
- accepting new patients
- Start Date
- Completion Date
- (estimated)
- Sponsor
- Nyra Medical, Inc.
- ID
- NCT07503236
- Study Type
- Interventional
- Participants
- Expecting 30 study participants
- Last Updated
Please contact me about this study
We will not share your information with anyone other than the team in charge of this study, which might include an external sponsor. Providing your contact details does not obligate you to participate in the research.
Thank you!
The study team should get back to you in a few business days.