This study is a prospective, multi-center, non-randomized first in human study to evaluate the safety and feasibility of the Capstan Medical TMVR System for intervention in adults with moderate-severe or greater mitral regurgitation who are not surgical candidates.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
DEVICE_FEASIBILITY
Masking
NONE
Enrollment
10
This is a first human use trial exploring a novel transcatheter mitral valve replacement implant and electro-mechanical delivery system. The device offers a minimally invasive repair for patients who have at symptomatic regurgitation who are otherwise ineligable for surgical intervention, or who have no other prospects for treatment and in whom medical therapy has already been optimised.
Monash Health, Victorian Heart Hospital
Melbourne, Australia
NOT_YET_RECRUITINGInstituto do Coração de São Paulo Incor
São Paulo, Brazil
NOT_YET_RECRUITINGPontificia Universidad Católica de Chile
Santiago, Chile
RECRUITINGIncidence of procedural success
Number of participants with successful valve deployment and freedom from death or re-hospitalization for heart failure at 30 days.
Time frame: Procedure through 30 days
Technical Success
Technical success is defined as successful Capstan Valve deployment with none/trace or mild mitral regurgitation at 30 days post- procedure.
Time frame: 30-Days
Freedom from MAE
Successful Capstan Valve Deployment with freedom from device- or procedure-related Major Adverse Events (MAE). MAE is a composite of the following device or procedure related outcomes: * All-cause mortality * Emergency cardiac or vascular surgery, or re-intervention * Myocardial Infarction * Stroke * Life-threatening bleeding
Time frame: 30-days, 90-days, 6-months, 1-year, then annually to 5-years
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Auckland City Hospital
Auckland, New Zealand
RECRUITING