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NCT02806570Completed

The CorCinch - Functional Mitral Valve Regurgitation (FMR) Study

Early Feasibility Study of the AccuCinch® Ventricular Restoration System

Source: ClinicalTrials.gov · Last updated 29 Jan 2025

Brief summary (registry, in English)

This is a multi-center, non-randomized, prospective Early Feasibility Study to evaluate the AccuCinch® Ventricular Restoration System in patients with symptomatic heart failure and concomitant functional mitral regurgitation that have stable symptoms on guideline-directed medical therapy

Status (registry)
Completed
Study type
Interventional
Enrollment
35 (actual)
First submitted
16 Jun 2016
Start date
1 Aug 2016
Primary completion date
31 Jan 2020
Lead sponsor
Ancora Heart, Inc.
NCT number
NCT02806570

What you commit to

  • Study type: Interventional
  • Participants enrolled: 35
  • From 1 Aug 2016 to the primary completion date, 31 Jan 2020
  • 16 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Prior surgical, transcatheter, or percutaneous mitral valve intervention
  • Anatomical pathology/constraints preventing appropriate access/implant of the AccuCinch® Ventricular Restoration System (e.g., femoral arteries will not support a 20F system)

Other illness

  • Myocardial infarction or any percutaneous cardiovascular intervention, cardiovascular surgery, or carotid surgery within 30 days
  • Untreated clinically significant coronary artery disease (CAD) requiring revascularization
  • Any planned cardiac surgery or interventions within the next 6 months (including right heart procedures)
  • NYHA class IV (i.e., non-ambulatory) or American College of Cardiology (ACC)/American Heart Association (AHA) Stage D heart failure
  • Hypertrophic cardiomyopathy, restrictive cardiomyopathy, constrictive pericarditis, or any other structural heart disease causing heart failure other than dilated cardiomyopathy of either ischemic or non-ischemic etiology.

Lab values

  • Renal insufficiency (i.e., eGFR of \<30ml/min/1.73m2; Stage 4 or 5 CKD)

Other

  • Patients with significant organic mitral valve pathology (e.g. myxomatous degeneration, mitral valve prolapse or flail leaflets)
  • Hemodynamic instability: Hypotension (systolic pressure \<90 mmHg) or requirement for inotropic support or mechanical hemodynamic support
  • Fixed pulmonary artery systolic pressure \>70 mmHg
  • Severe tricuspid regurgitation (per ASE guidelines and graded by the Echo Core Lab)
  • Modified Rankin Scale ≥ 4 disability
  • Moderate or severe aortic valve stenosis or regurgitation or aortic valve prosthesis
  • Fluoroscopic or echocardiographic evidence of severe aortic arch calcification, mobile aortic atheroma, intracardiac mass, thrombus or vegetation
  • Active bacterial endocarditis

Who the study is looking for

  • Study patient is at least 18-years old
  • Severity of FMR: ≥ Moderate (i.e., 2+, according to Stone et al Clinical Trial Design Principles and Endpoint Definitions for Transcatheter Mitral Valve Repair and Replacement: Part 1: Clinical Trial Design Principles. A Consensus Document from the Mitral Valve Academic Research Consortium11; and 2003 ASE Guidelines for grading mitral regurgitation10)
  • Ejection Fraction: ≥20 to ≤60%
  • Symptom Status: NYHA II-IV (i.e., ambulatory)
  • Treatment and compliance with optimal guideline directed medical therapy for heart failure for at least 1 month
  • Surgical risk: Subject is eligible for cardiac surgery (specific risk score or comorbidities should demonstrate high risk features, as determined by the Heart Team)
  • Completion of all qualifying diagnostic and functional tests and agrees to comply with study follow-up schedule

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (16)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Emory University
Coordinator of this site? Confirm its status
AtlantaUnited StatesUnknown status
University of Virginia School of Medicine
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CharlottesvilleUnited StatesUnknown status
The Christ Hospital
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CincinnatiUnited StatesUnknown status
Pinnacle Health Cardiovascular Institute
Coordinator of this site? Confirm its status
HarrisburgUnited StatesUnknown status
Penn State Health Milton S. Hershey Medical Center
Coordinator of this site? Confirm its status
HersheyUnited StatesUnknown status
Baylor College of Medicine St. Luke's Medical Center
Coordinator of this site? Confirm its status
HoustonUnited StatesUnknown status
Nebraska Heart Institute / Nebraska Heart Hospital
Coordinator of this site? Confirm its status
LincolnUnited StatesUnknown status
University of Louisville
Coordinator of this site? Confirm its status
LouisvilleUnited StatesUnknown status
Minneapolis Heart Foundation Institute
Coordinator of this site? Confirm its status
MinneapolisUnited StatesUnknown status
Columbia University Medical Center
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New YorkUnited StatesUnknown status
NYU Langone Medical Center
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New YorkUnited StatesUnknown status
Carilion Medical Center
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RoanokeUnited StatesUnknown status
Intermountain Medical Center
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Salt Lake CityUnited StatesUnknown status
University of Washington Medicine
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SeattleUnited StatesUnknown status
Barnes-Jewish Hospital
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St LouisUnited StatesUnknown status
Montefiore Medical Center
Coordinator of this site? Confirm its status
The BronxUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.