Effectiveness of Surgical Mitral Valve Repair Versus Medical Treatment for People With Significant Mitral Regurgitation and Non-ischemic Congestive Heart Failure

Heart Failure Clinical Trial

— SMMART-HF  

Official title:

Surgery Versus Medical Treatment Alone for Patients With Significant Mitral Regurgitation and Non-ischemic Congestive Heart Failure: SMMART-HF

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT00608140
• Other study ID #: Pro00002860
• Secondary ID: U01HL084904
• Status: Terminated
• Phase: Phase 3
• First received: January 24, 2008
• Last updated: March 9, 2018
• Start date: March 2008
• Est. completion date: March 2010

Study information

• Verified date: July 2013
• Source: Duke University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Mitral regurgitation (MR), also known as mitral insufficiency, is a condition in which the heart's mitral valve, located between two of the heart's main chambers, does not firmly shut, allowing blood to leak backwards within the heart. Improper functioning of the mitral valve disrupts the proper flow of blood through the body, resulting in shortness of breath and fatigue. When mild, MR may not pose a significant danger to a person's health, but severe MR may be associated with serious complications, such as heart failure, irregular heart rhythm, and high blood pressure. Although there are treatments for MR, including medication and surgery, more information is needed on the effectiveness of these treatments in people with significant MR. This study will compare the safety and effectiveness of corrective surgery added to optimal medical treatment (OMT) versus OMT alone in treating people with significant MR caused by an enlarged heart.

Description:

It is estimated that approximately 4 out of 10 people with an enlarged heart due to heart failure develop MR, referred to as secondary MR. This type of MR is caused by enlargement of the left ventricle (LV), one of the heart's main chambers. In turn, the enlargement leads to stretching of certain heart muscles around the mitral valve and of the valve itself. Symptoms of secondary MR may include shortness of breath, fatigue, dizziness, swollen feet, cough, and heart palpitations. Mitral valve repair or replacement surgery is sometimes considered as a treatment option to restore proper heart function in people with secondary MR. Surgical repair with placement of an artificial ring around the mitral valve can help to tighten the valve and add benefit to non-surgical treatments for MR. However, although surgical placement of the ring improves mitral valve function in most people, it is not known whether this surgery helps people live longer and healthier lives. This study will compare the safety and effectiveness of surgical mitral valvuloplasty with placement of an annular ring (SMVR) added to optimal medical treatment (OMT) versus OMT alone in non-ischemic heart failure patients with significant secondary MR.

Participation from baseline through follow-up in this study will last 18 months. All potential participants will initially undergo a transesophageal echocardiogram to confirm the presence of an abnormal mitral valve. Eligible participants will then undergo a number of baseline tests, which will include cardiopulmonary exercise stress testing, a chest wall echocardiogram, blood draw, 6-minute walk test, medical questionnaires, and a physical exam. Next, participants will be randomly assigned to receive immediate open heart surgery with the placement of a mitral valve ring, delayed surgery at least 18 months later, or OMT. Participants assigned to receive immediate surgery will undergo the surgery 2 weeks after baseline testing. Participants assigned to receive OMT will receive treatment with any of the following medication regimens: combination of vasodilator therapy and diuretics, nitrates and nifedipine, and beta-adrenergic blocker therapy. Follow-up visits for all participants will occur at Months 1, 3, 6, 12, and 18 and will include repeat baseline testing. Long-term survival status data may be collected beyond 18 months for some participants.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 2
• Est. completion date: March 2010
• Est. primary completion date: March 2010
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Symptomatic chronic heart failure, New York Heart Association (NYHA) class II to IIIb

• Left ventricular ejection fraction of 0.35 due to non-ischemic etiology

• Evidence by transthoracic echocardiography (TTE) of moderate or severe MR without obvious primary mitral valve pathology

• Peak VO2 less than or equal to 22 ml/kg/min, as obtained at study entry

• Optimal heart failure therapy for at least 6 months prior to study entry

Exclusion Criteria:

• Significant coronary artery disease (greater than 75% lesion in any vessel) by coronary angiography or by a history of a prior heart attack

• Heart failure due to active myocarditis, congenital heart disease, or obstructive hypertrophic cardiomyopathy

• Significant ventricular arrhythmias not treated with an implantable defibrillator

• Primary MR due to significant chordal or leaflet abnormalities by TTE

• Other hemodynamically relevant stenotic or regurgitant valvular diseases

• Severe tricuspid regurgitation (TR) (moderate TR is allowed)

• Severe pulmonic regurgitation (PR) (moderate PR is allowed)

• Moderate to severe aortic regurgitation

• Any moderate to severe stenotic lesions using American Heart Association/American College of Cardiology (AHA/ACC) criteria 31

• Dependence on chronic inotropic therapy

• Restrictive cardiomyopathy or constrictive pericarditis

• Severe right ventricular dysfunction

• Baseline creatinine greater than or equal to 3 mg/dL or renal replacement therapy (chronic hemodialysis or peritoneal dialysis)

• Poor transthoracic sonographic windows precluding reasonable assessment of LV endocardial borders from apical imaging on TTE

• Inability to perform the spirometric exercise testing

• Significant chronic lung disease that might interfere with the ability to interpret the spirometric measurements, including home oxygen, forced expiratory volume in 1 second (FEV1) less than 1.0 L/min, or exertional hypoxemia with saturations less than 90%

• Any known neoplastic disease other than skin cancer

• Other terminal illness with a life expectancy less than 1 year

• Plan for percutaneous mitral valve procedure

Related Conditions & MeSH terms

• Heart Failure
• Mitral Valve Insufficiency

Intervention

Procedure:
• Surgical mitral valvuloplasty with placement of annular ring (SMVR)
Participants will undergo open heart surgery to mechanically reduce mitral regurgitation (MR). A complete rigid or semi-rigid annular ring will be placed unless specifically contraindicated by intraoperative findings. The ring size will be between 24 mm and 27 mm in the anteroposterior diameter. Annular ring sutures will be placed circumferentially approximately 1 mm off the hinge point between the leaflet and the atrial tissue. The total number of sutures will vary between 4 and 7 sutures anteriorly, while 8 to 12 sutures will be utilized for the posterior segment of the annulus. Additional repair of the mitral apparatus itself will be based on intraoperative findings. Leaflet repair will be performed for significant prolapse. Submitral apparatus repair will be performed for ruptured or significantly elongated chordae as well as significant chordal tethering.

Drug:
• Optimal medical therapy (OMT)
Optimal medical therapy can include, but is not limited to, any of the following treatment regimens: combination of vasodilator therapy and diuretics, nitrates and nifedipine, and beta-adrenergic blocker therapy.

Locations

Country	Name	City	State
Canada	Montreal Heart Institute	Montreal	Quebec
United States	Morehouse School of Medicine	Atlanta	Georgia
United States	Brigham and Women's Hospital	Boston	Massachusetts
United States	University of Vermont - Fletcher Allen Health Care	Burlington	Vermont
United States	Duke University Medical Center	Durham	North Carolina
United States	Baylor College of Medicine	Houston	Texas
United States	Minnesota Heart Failure Network	Minneapolis	Minnesota
United States	University of Utah Health Sciences Center	Murray	Utah
United States	Mayo Clinic	Rochester	Minnesota

Sponsors (3)

Lead Sponsor	Collaborator
Duke University	Heart Failure Clinical Research Network, National Heart, Lung, and Blood Institute (NHLBI)

Countries where clinical trial is conducted

United States,  Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Effect of Adding SMVR to OMT Alone on LV Remodeling, Specifically LV End-systolic Volume Index (LVESVI)		Measured at Month 18
Secondary	Peak VO2		Measured at Month 18
Secondary	Change in 6-minute Walk Test	The 2 patients enrolled did not meet the 18 month measurement of primary/secondary endpoints before the trial was terminated. No data were collected for this outcome measure and no analysis was performed.	Measured at baseline and Month 18 but n/a
Secondary	Change in Minnesota Living With Heart Failure (MLHF) Score	Change in MLHF score. However, the 2 patients enrolled did not meet the 18 month measurement of primary/secondary endpoints before the trial was terminated. No analysis was performed.	Planned to be measured at baseline and Month 18 but n/a
Secondary	Total Days Alive and Total Days Not Hospitalized	Total days alive and not hospitalized by 18 months. However, the 2 patients enrolled did not meet the 18 month measurement of primary/secondary endpoints before the trial was terminated. No analysis was performed.	Measured at baseline and Month 18
Secondary	Total Mortality (All Causes)	Total all-cause mortality at 18 months. However, the 2 patients enrolled did not meet the 18 month measurement of primary/secondary endpoints before the trial was terminated. No analysis was performed.	Measured at Month 18
Secondary	Perioperative Mortality		Measured between Days 0 and 30 postsurgery