Mandibular Advancement to Reduce Ventricular Load and Improve Quality-of-life in Heart Failure

Starting soon · Not applicable · Has a placebo group

Conditions studied: Heart Failure, OSA - Obstructive Sleep Apnea

In brief

Heart failure with reduced ejection fraction (HFrEF) is a serious condition that limits daily activities and often leads to hospital stays and early death. Many patients with HFrEF also have obstructive sleep apnea (OSA), a common but often undiagnosed condition where breathing repeatedly stops during sleep. This causes drops in oxygen, poor sleep, and stress on the heart, which can make heart failure worse. The investigators are studying whether a device called a mandibular advancement device (MAD)-a mouthpiece worn during sleep that keeps the airway open-can help people with both HFrEF and moderate-to-severe OSA. This device is already approved to treat OSA and is often more comfortable and easier to use than a CPAP machine. In our study, 328 patients in Singapore will be randomly assigned to use either the MAD or a sham device that looks the same but doesn't move the jaw. They will wear the device for 12 months. We will measure changes in a blood marker linked to heart failure severity, as well as exercise ability, blood pressure, sleep quality, and hospital visits. The investigators hope this study will show that MAD is a simple and patient-friendly way to improve outcomes in people with heart failure.

Key facts

Study ID: NCT07460505
Run by: National University Hospital, Singapore
People needed: 328
Starts: 2026-05-01
Expected to finish: 2031-04-01
Last updated by the study team: 2026-03-10

Who can join

Age: 40 and older, up to 99. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Age of at least 40 years old with the capacity to provide signed, written informed consent
Ischemic or non-ischemic cardiomyopathy with a left ventricular ejection fraction of 20% to 40% in the previous 6 months
Stable chronic HF with NYHA functional class I-III symptoms on maximally tolerated background therapy for at least 4 weeks
NT-proBNP >600 pg/mL (for participants in sinus rhythm) or >900 pg/mL (for participants in atrial fibrillation) in the previous 6 months (same as leading HF trials)
Agree to follow the study protocol
Able and willing to undergo a hospital-based overnight polysomnography

You may not qualify if…

Known OSA and already on regular treatment
Moderate or severe valvular stenosis or regurgitation
Severe hypoxemia on polysomnography ODI >60 or min SpO2 <60%
Specific HF etiologies, including hypertrophic cardiomyopathy with left ventricular outflow tract obstruction; pericardial disease; infiltrative or inflammatory myocardial disease; valvular heart disease with severe aortic or primary mitral regurgitation, moderate or severe aortic stenosis, any mitral stenosis requiring surgical repair, or active endocarditis
Contraindications to MAD: less than six teeth in each arch; inability to advance the mandible and open the jaw widely.
Pre-existing temporomandibular joint problems, severe bruxism, and advanced periodontal disease (with mobility affecting MAD stability).
Patients who are planning to have restorations, dental prostheses or implants done in the next 12 months
Limited life expectancy (< one year)
Cardiac or cerebrovascular events in the past 6 months, including myocardial infarction, unstable angina leading to hospitalization, uncontrolled cardiac arrhythmia, carotid surgery or stenting, stroke, transient ischemic attack, carotid revascularization, endovascular procedure, or surgical intervention for peripheral vascular disease
Current or planned mechanical circulatory support or heart transplantation Current or planned (within the next 6 months) hemodialysis or peritoneal dialysis

Where it is running

National University Hospital — Singapore, Kent Ridge, Singapore

Full record on ClinicalTrials.gov

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