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Clinical Trials/NCT02985268
NCT02985268
Withdrawn
Not Applicable

Evaluation of Outcomes of Cardiac Resynchronization Therapy and MitraClip for the Treatment of Low Ejection Fraction and Functional Mitral Valve Regurgitation in Heart Failure

Montreal Heart Institute0 sitesDecember 2016

Overview

Phase
Not Applicable
Intervention
MitraClip
Conditions
Functional Mitral Regurgitation
Sponsor
Montreal Heart Institute
Primary Endpoint
Improvement in distance walked on a six-minute walk test (6MWT)
Status
Withdrawn
Last Updated
6 years ago

Overview

Brief Summary

At present, the optimal treatment strategy for heart failure patients and moderate-to-severe (3+) or severe (4+) mitral regurgitation with a class IIa recommendation for CRT is uncertain.Whether these patents should also be treated for functional mitral regurgitation or with CRT also remains unclear. We therefore propose a randomized 2x2 factorial design in this patient population to understand the the impact of both CRT and transcatheter mitral valve repair with the MitraClip on their functional status and quality of life.

Registry
clinicaltrials.gov
Start Date
December 2016
End Date
February 2020
Last Updated
6 years ago
Study Type
Interventional
Study Design
Factorial
Sex
All

Investigators

Sponsor
Montreal Heart Institute
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Symptomatic moderate-to-severe (3+) or severe (4+) functional mitral regurgitation due to cardiomyopathy of either ischemic or non-ischemic etiology as determined by transthoracic echocardiogram (TTE), and confirmed by the Echocardiography Core Lab (ECL);
  • Symptomatic heart failure as defined by New York Heart Association (NYHA) class II, III or ambulatory IV;
  • Treatment and compliance with optimal medical therapy for heart failure for at least 30 days; Optimal medical therapy is defined by: Maximum tolerated beta-blocker, angiotensin converting enzyme inhibitor (ACE) or angiotensin receptor blocker (ARB), and aldosterone antagonist (as per the ACCF/AHA Guidelines as judged by the HF specialist investigator on site and confirmed by the Clinical Eligibility Committee).
  • Left ventricular ejection fraction ≤ 35%, as assessed by any one of the following methods: echocardiography, contrast left ventriculography, gated blood pool scan or cardiac magnetic resonance imaging (MRI);
  • Class IIa indication for cardiac resynchronization therapy:
  • Left bundle branch block (LBBB) and QRS duration of 120-149 ms;
  • Right bundle branch block (RBBB) and QRS ≥ 150 ms.
  • Clinical agreement amongst local investigators that the patient will not be offered surgical intervention;
  • The primary regurgitant jet, in the opinion of the MitraClip implanting investigator, can successfully be treated by the MitraClip. Treatment of commissural mitral regurgitation may be treated at the discretion of the operator. All major jets contributing the secondary MR will be treated with the MitraClip;
  • Ability to perform a six-minute walk test (6MWT) without substantial physical limitations and without use of a walker or wheelchair and distance walked in 6 minutes of ≤ 450m;

Exclusion Criteria

  • Life expectancy less than 12 months due to noncardiac conditions;
  • ACC/AHA Stage D Heart Failure;
  • Left ventricular ejection fraction ≤ 15%;
  • Hypotension (systolic pressure \<90 mm Hg) or requirement for inotropic support or mechanical hemodynamic support;
  • United Network for Organ Sharing (UNOS) status 1 heart transplantation or prior orthotopic heart transplantation;
  • Untreated clinically significant coronary artery disease requiring revascularization;
  • CABG within prior 30 days;
  • Percutaneous coronary intervention within prior 30 days;
  • Severe Chronic Obstructive Pulmonary Disease (COPD) requiring continuous daytime home oxygen or chronic oral corticosteroid therapy;
  • Previous surgical mitral valve bioprosthesis, mitral annuloplasty, or transcatheter mitral valve procedure;

Arms & Interventions

MitraClip/Optimal Medical Therapy (OMT) and CRT ON

Patient to be implanted with both MitraClip and CRT-D. Will also receive optimal medical therapy. CRT-D will be programmed to ON

Intervention: MitraClip

MitraClip/Optimal Medical Therapy (OMT) and CRT ON

Patient to be implanted with both MitraClip and CRT-D. Will also receive optimal medical therapy. CRT-D will be programmed to ON

Intervention: Optimal Medical Therapy

MitraClip/Optimal Medical Therapy (OMT) and CRT ON

Patient to be implanted with both MitraClip and CRT-D. Will also receive optimal medical therapy. CRT-D will be programmed to ON

Intervention: CRT-D

MitraClip/OMT and CRT OFF

Patient to be implanted with both MitraClip and CRT-D. Will also receive optimal medical therapy. CRT-D will be programmed to OFF until the 6-month follow-up visit in which the CRT will be turned ON

Intervention: MitraClip

MitraClip/OMT and CRT OFF

Patient to be implanted with both MitraClip and CRT-D. Will also receive optimal medical therapy. CRT-D will be programmed to OFF until the 6-month follow-up visit in which the CRT will be turned ON

Intervention: Optimal Medical Therapy

MitraClip/OMT and CRT OFF

Patient to be implanted with both MitraClip and CRT-D. Will also receive optimal medical therapy. CRT-D will be programmed to OFF until the 6-month follow-up visit in which the CRT will be turned ON

Intervention: CRT-D

OMT and CRT ON

Patient to be implanted with only the CRT-D and will receive optimal medical therapy. CRT-D will be programmed to ON

Intervention: Optimal Medical Therapy

OMT and CRT ON

Patient to be implanted with only the CRT-D and will receive optimal medical therapy. CRT-D will be programmed to ON

Intervention: CRT-D

OMT and CRT OFF

Patient to be implanted with only the CRT-D and will receive optimal medical therapy. CRT-D will be programmed to OFF until the 6-month follow-up visit in which the CRT will be turned ON

Intervention: Optimal Medical Therapy

OMT and CRT OFF

Patient to be implanted with only the CRT-D and will receive optimal medical therapy. CRT-D will be programmed to OFF until the 6-month follow-up visit in which the CRT will be turned ON

Intervention: CRT-D

Outcomes

Primary Outcomes

Improvement in distance walked on a six-minute walk test (6MWT)

Time Frame: Baseline to 6 months

Secondary Outcomes

  • Change in cardiographic endpoints(Baseline to 6 months)
  • Change in Quality of Life Assessment scores(Baseline to 6 months)
  • Number of Re-hospitalizations for decompensated heart failure(6 and 12 months)

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