Cardiovascular disease remains the leading cause of death worldwide, but treatment has advanced dramatically. Statins, blood pressure medications, and antiplatelet drugs prevent millions of heart attacks and strokes annually. Research now focuses on inflammation, lipid targets beyond LDL cholesterol, and genetic forms of heart disease.
What's actually going on in research
Trials are testing PCSK9 inhibitors and RNA-based therapies for cholesterol, anti-inflammatory drugs that reduce heart attack risk, SGLT2 inhibitors and GLP-1 receptor agonists originally developed for diabetes, and gene therapies for familial hypercholesterolemia. Researchers are also studying heart failure with preserved ejection fraction, where few treatments have worked until recently.
Anti-inflammatory approaches
Studies show that inflammation drives heart disease independently of cholesterol. Drugs targeting interleukin-6 and other inflammatory pathways are being tested to prevent heart attacks in people with high inflammation markers.
RNA therapeutics
Inclisiran, an RNA drug given twice yearly by injection, lowers LDL cholesterol by silencing the PCSK9 gene in the liver. Other RNA drugs targeting lipoprotein(a), a stubborn genetic cholesterol particle, are in late-stage trials.
Heart failure advances
SGLT2 inhibitors and finerenone have shown benefit in heart failure, expanding options beyond traditional diuretics and beta-blockers. Trials are testing whether these drugs work in people with preserved ejection fraction, where the heart pumps normally but stiffens.
What to know before you search
Eligibility typically depends on cholesterol levels, blood pressure, history of heart attack or stroke, heart function measurements, and current medications.
What types of trials are currently open
- Prevention trials — Testing cholesterol-lowering drugs, blood pressure medications, or antiplatelet therapies to prevent first or recurrent heart attacks and strokes.
- Heart failure trials — Studies of drugs or devices for people whose hearts pump weakly or have stiffened, often comparing new treatments to standard diuretics and beta-blockers.
- Intervention trials — Testing catheter-based procedures or new stent designs for blocked arteries, often comparing them to bypass surgery or medication alone.
- Arrhythmia trials — Studies of drugs or ablation procedures for atrial fibrillation and other rhythm problems, often measuring stroke risk and quality of life.
- Imaging studies — Using advanced scans to measure plaque buildup, inflammation, or heart muscle scarring, helping identify who needs more aggressive treatment.
Recently added Cardiovascular Disease trials
Take a weekly injection to test a new diabetes treatment
This study is being conducted to find out how well zenagamtide works and how safe it is compared to insulin glargine in participants with type 2 diabetes who are at higher risk of heart and blood vessel problems and are already taking 1 to 3 diabetes medications. There are 2 study treatments in this study taken as injections under the skin once a week. Participants will either get zenagamtide, (the treatment being tested) or insulin glargine (a comparator) and which treatment participants get is decided by chance.
Digital Intelligent Tongue-Pressure Biofeedback Resistance Training for Post-Stroke Dysphagia: A Randomized Controlled Trial
Post-stroke dysphagia is a common complication of stroke and may lead to impaired oral intake, malnutrition, aspiration, and pneumonia. Reduced tongue strength and tongue pressure are important contributors to impaired swallowing after stroke. Conventional tongue-pressure resistance training may improve tongue strength, but traditional training provides limited real-time feedback and may be difficult to individualize.This prospective, multicenter, randomized, open-label, parallel-controlled trial will evaluate the effectiveness of digital intelligent tongue-pressure biofeedback resistance training in patients with post-stroke dysphagia. A total of 80 participants will be randomly assigned in a 1:1 ratio to an intervention group or a control group. Participants in the intervention group will receive digital intelligent tongue-pressure biofeedback resistance training in addition to conventional swallowing rehabilitation, while participants in the control group will receive conventional rehabilitation without the digital biofeedback intervention. The intervention period will last 2 weeks.Swallowing function will be assessed at baseline and after completion of the intervention. The primary outcome is the change in Functional Oral Intake Scale (FOIS) score. Secondary assessments include maximum tongue pressure and quantitative videofluoroscopic swallowing study (VFSS) measures, including oral transit time, Penetration-Aspiration Scale score, and pharyngeal residue. The study aims to determine whether digital intelligent tongue-pressure biofeedback resistance training provides additional benefits for swallowing function, tongue strength, and swallowing safety in patients with post-stroke dysphagia.
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