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| Name | Class |
|---|---|
| Abbott Medical Devices | INDUSTRY |
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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.
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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Guideline-directed medical therapy | Placebo Comparator | Standard guideline-directed medical treatment for heart failure |
|
| Transcatheter Mitral valve repair | Experimental | MitraClip treatment |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Transcatheter mitral valve repair | Device | Transcatheter mitral valve repair performed using the MitraClip device |
|
| Measure | Description | Time Frame |
|---|---|---|
| Left ventricular diastolic remodelling | Change in indexed left ventricular diastolic volume (LVEDV) | 12 months |
| Functional capacity as measured by 6 minute walk test | Change in distance walked on six-minute walk test | 12 months |
| Measure | Description | Time Frame |
|---|---|---|
| Mitral regurgitation Severity (RV) | Change in mitral regurgitant volume | 12 months |
| Mitral regurgitation Severity (EROA) | Change in effective regurgitant orifice area |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Anita W Asgar, MD | Contact | 5143763330 | 3800 | anita.asgar@umontreal.ca |
| Name | Affiliation | Role |
|---|---|---|
| Anita W Asgar, MD | Montreal Heart Institute | Principal Investigator |
| Anique Ducharme, MD | Montreal Heart Institute | Principal Investigator |
| Jean L Rouleau, MD |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Montreal Heart Institute | Recruiting | Montreal | Quebec | H1T1C8 | Canada |
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| ID | Term |
|---|---|
| D008944 | Mitral Valve Insufficiency |
| D006333 | Heart Failure |
| ID | Term |
|---|---|
| D006349 | Heart Valve Diseases |
| D006331 | Heart Diseases |
| D002318 | Cardiovascular Diseases |
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Patients will be randomized 1:1 to medical treatment or intervention with the MitraClip device
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| Guideline-directed medical therapy | Other | Standard medical therapy for heart failure as recommended by HF guidelines |
|
| 12 months |
| 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. | 12 months |
| Montreal Heart Institute |
| Study Chair |