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MitraClip for the Treatment of Moderate Functional Mitral Regurgitation: EVOLVE-MR (EVOLVE-MR)

Primary Purpose

Mitral Regurgitation, Heart Failure, Mitral Valve Regurgitation Due to Cardiomyopathy (Disorder)

Status
Unknown status
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Transcatheter mitral valve repair
Guideline-directed medical therapy
Sponsored by
Montreal Heart Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Mitral Regurgitation focused on measuring mitral regurgitation, transcatheter mitral valve repair

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Moderate functional mitral regurgitation (2+, 2-3+)
  • Left ventricular ejection fraction >20%
  • LVEDV 75-110 ml/m2
  • Symptomatic heart failure (NYHA Class II-IV)

Exclusion Criteria:

  • Left ventricular ejection fraction < 20%
  • Severe functional mitral regurgitation
  • Recent coronary artery bypass graft surgery (CABG)
  • Untreated significant coronary artery disease
  • Mitral valve area < 4.0cm2
  • Severe pulmonary hypertension

Sites / Locations

  • Montreal Heart InstituteRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Experimental

Arm Label

Guideline-directed medical therapy

Transcatheter Mitral valve repair

Arm Description

Standard guideline-directed medical treatment for heart failure

MitraClip treatment

Outcomes

Primary Outcome Measures

Left ventricular diastolic remodelling
Change in indexed left ventricular diastolic volume (LVEDV)
Functional capacity as measured by 6 minute walk test
Change in distance walked on six-minute walk test

Secondary Outcome Measures

Mitral regurgitation Severity (RV)
Change in mitral regurgitant volume
Mitral regurgitation Severity (EROA)
Change in effective regurgitant orifice area
Quality of Life Measurement
Change in indices of quality of life as measured by Kansas City Cardiomyopathy Questionnaire. The Kansas City Cardiomyopathy Questionnaire is a 23-item, self-administered instrument that quantifies physical function, symptoms (frequency, severity and recent change), social function, self-efficacy and knowledge, and quality of life. In the KCCQ, an overall summary score can be derived from the physical function, symptom (frequency and severity), social function and quality of life domains. For each domain, the validity, reproducibility, responsiveness and interpretability have been independently established. Scores are transformed to a range of 0-100, in which higher scores reflect better health status.

Full Information

First Posted
August 4, 2018
Last Updated
August 12, 2019
Sponsor
Montreal Heart Institute
Collaborators
Abbott Medical Devices
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1. Study Identification

Unique Protocol Identification Number
NCT03705312
Brief Title
MitraClip for the Treatment of Moderate Functional Mitral Regurgitation: EVOLVE-MR
Acronym
EVOLVE-MR
Official Title
EValuation of Outcomes of Transcatheter Mitral Valve Repair for the Treatment of Low Ejection Fraction and Moderate Functional Mitral ValvE Regurgitation In Heart Failure
Study Type
Interventional

2. Study Status

Record Verification Date
October 2018
Overall Recruitment Status
Unknown status
Study Start Date
February 22, 2019 (Actual)
Primary Completion Date
December 2021 (Anticipated)
Study Completion Date
January 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Montreal Heart Institute
Collaborators
Abbott Medical Devices

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study evaluates the addition of transcatheter mitral valve repair with the MitraClip device to medical treatment in patients with heart failure and moderate functional mitral regurgitation to determine the impact of left ventricular remodelling and patients' functional capacity.
Detailed Description
Moderate mitral regurgitation in patients with LV dysfunction is associated with increased risk of death and hospitalizations for heart failure (HF) and leads to progressive remodelling of an already damaged left ventricle. Medical therapies and cardiac resynchronization therapy (CRT) have demonstrated favourable effects on LV remodelling in heart failure patients. Given the benefits and safety of transcatheter mitral valve repair with the MitraClip device in severe MR, it is conceivable that this technology could also be safely used in those with moderate MR to reduce mitral regurgitation, improve symptoms and result in LV remodelling. At present, the optimal treatment strategy for heart failure patients and moderate (2+, 2-3+) mitral regurgitation is uncertain therefore the EVOLVE-MR study proposes to evaluate transcatheter mitral valve repair with the MitraClip in such patients to study the effects on LV remodelling and functional capacity. EVOLVE-MR is a randomized study of MitraClip and medical therapy in symptomatic heart failure patients with moderate (2+, 2-3+) secondary mitral regurgitation. The objective of this study is to determine the impact of both therapies on left ventricular remodelling and functional capacity of the target patient population.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Mitral Regurgitation, Heart Failure, Mitral Valve Regurgitation Due to Cardiomyopathy (Disorder)
Keywords
mitral regurgitation, transcatheter mitral valve repair

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Patients will be randomized 1:1 to medical treatment or intervention with the MitraClip device
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
174 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Guideline-directed medical therapy
Arm Type
Placebo Comparator
Arm Description
Standard guideline-directed medical treatment for heart failure
Arm Title
Transcatheter Mitral valve repair
Arm Type
Experimental
Arm Description
MitraClip treatment
Intervention Type
Device
Intervention Name(s)
Transcatheter mitral valve repair
Other Intervention Name(s)
MitraClip
Intervention Description
Transcatheter mitral valve repair performed using the MitraClip device
Intervention Type
Other
Intervention Name(s)
Guideline-directed medical therapy
Intervention Description
Standard medical therapy for heart failure as recommended by HF guidelines
Primary Outcome Measure Information:
Title
Left ventricular diastolic remodelling
Description
Change in indexed left ventricular diastolic volume (LVEDV)
Time Frame
12 months
Title
Functional capacity as measured by 6 minute walk test
Description
Change in distance walked on six-minute walk test
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Mitral regurgitation Severity (RV)
Description
Change in mitral regurgitant volume
Time Frame
12 months
Title
Mitral regurgitation Severity (EROA)
Description
Change in effective regurgitant orifice area
Time Frame
12 months
Title
Quality of Life Measurement
Description
Change in indices of quality of life as measured by Kansas City Cardiomyopathy Questionnaire. The Kansas City Cardiomyopathy Questionnaire is a 23-item, self-administered instrument that quantifies physical function, symptoms (frequency, severity and recent change), social function, self-efficacy and knowledge, and quality of life. In the KCCQ, an overall summary score can be derived from the physical function, symptom (frequency and severity), social function and quality of life domains. For each domain, the validity, reproducibility, responsiveness and interpretability have been independently established. Scores are transformed to a range of 0-100, in which higher scores reflect better health status.
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Moderate functional mitral regurgitation (2+, 2-3+) Left ventricular ejection fraction >20% LVEDV 75-110 ml/m2 Symptomatic heart failure (NYHA Class II-IV) Exclusion Criteria: Left ventricular ejection fraction < 20% Severe functional mitral regurgitation Recent coronary artery bypass graft surgery (CABG) Untreated significant coronary artery disease Mitral valve area < 4.0cm2 Severe pulmonary hypertension
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Anita W Asgar, MD
Phone
5143763330
Ext
3800
Email
anita.asgar@umontreal.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anita W Asgar, MD
Organizational Affiliation
Montreal Heart Institute
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Anique Ducharme, MD
Organizational Affiliation
Montreal Heart Institute
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jean L Rouleau, MD
Organizational Affiliation
Montreal Heart Institute
Official's Role
Study Chair
Facility Information:
Facility Name
Montreal Heart Institute
City
Montréal
State/Province
Quebec
ZIP/Postal Code
H1T1C8
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Anita W Asgar, MD
Phone
5143763330
Email
anita.asgar@umontreal.ca

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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MitraClip for the Treatment of Moderate Functional Mitral Regurgitation: EVOLVE-MR

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