Novel Technologies to Improve Echocardiographic Estimates of Left Ventricular Filling Pressure in Heart Failure Combined With Atrial Fibrillation
Condition(s) studied
Study summary
Heart failure and atrial fibrillation are two of the most common heart diseases globally. Nearly half of all patients with heart failure also have atrial fibrillation. When heart failure and atrial fibrillation occur together, the risk of hospitalization and premature death increases significantly. However, there is a lack of reliable tools to assess how severely the heart is affected in these patients. This makes it difficult both to establish the correct diagnosis, tailor treatment, and predict who is at greatest risk of hospital admission or death from the disease.
One of the most important targets in heart failure is the filling pressure in the left ventricle. When this pressure is high, it means that the heart has difficulty receiving blood, leading to shortness of breath and fluid retention in the body. Today, filling pressure is usually estimated using ultrasound (echocardiography), but the available methods are primarily developed for patients without atrial fibrillation. In patients with both heart failure and atrial fibrillation, the measurements are so uncertain that they cannot be used as a reliable basis for clinical decision-making.
In this study, entitled Heart Failure combined with Atrial Fibrillation (HFcAF), the investigators will test new ultrasound methods that combine novel measures of cardiac chamber function with established techniques. Artificial intelligence will be used to identify the most useful combinations of parameters, select cardiac cycles that are best suited for analysis in atrial fibrillation, and automate and optimize the measurements. This approach may provide both more accurate and faster assessments, while also making the methods easier to implement in clinical practice. The aim is to improve the estimation of filling pressure so that it becomes more precise also in patients with atrial fibrillation. The investigators will then examine whether these improved methods can be used to predict which patients are at highest risk of hospitalization or death due to heart failure.
The study is designed as a prospective multicenter study, in which patients are recruited from several hospitals in different countries. This will make the results robust and generalizable to a wide range of patient populations. The investigators anticipate that the project will pave the way for better diagnostics and risk stratification in heart failure combined with atrial fibrillation and, in the longer term, contribute to improved guidelines and treatment for a large number of patients. If successful, the project will provide a new tool that can contribute to earlier and more targeted treatment, thereby improving quality of life and prognosis for a large group of patients.
Eligibility
Primary outcome measure(s)
- Diagnostic accuracy of a non-invasive algorithm for classification of left ventricular filling pressure in atrial fibrillation — • Start recruitment: February 2026 • End recruitment: January 2028 • Follow-up: 3 years • Data analysis: Ferbuary 2026 - December 2028. Outcome analysis will be extended to 3 years of follow-up. • Manuscript preparation: December 2028 - December 2029
Main aim of the study is to develop and validate a clinically applicable algorithm combining echocardiographic and clinical parameters to differentiate normal from elevated LV filling pressure in AF with ≥80% diagnostic accuracy. Left venticular filling pressures will be measured during right- or left-sided heart catehterization and left ventricular filling pressure \>15 mmHg will be considered elevated. - Imaging markers associated with mortality and heart-failure hospitalization in atrial fibrillation — • Start recruitment: February 2026 • End recruitment: January 2028 • Follow-up: 3 years • Data analysis: Ferbuary 2026 - December 2028. Outcome analysis will be extended to 3 years of follow-up. • Manuscript preparation: December 2028 - December 2029
To identify prognostic imaging markers associated with mortality and heart-failure hospitalization over a 3-year follow-up period.
Trial sites (15)
| Facility | City | Region | Status |
|---|---|---|---|
| Cleveland Clinic | Cleveland | Ohio | Not Yet Recruiting |
| Methodist DeBakey Heart and Vascular Center | Houston | Texas | Not Yet Recruiting |
| Cardiovascular Center Aalst, OLV Clinic, Aalst, Belgium | Aalst | Belgium | Not Yet Recruiting |
| Catholic University of Leuven | Leuven | Belgium | Not Yet Recruiting |
| Laboratory Signal Processing and Image, Department of Cardiology | Rennes | France | Not Yet Recruiting |
| Service de Cardiologie, Hôpitaux Universitaires de Strasbourg | Strasbourg | France | Not Yet Recruiting |
| Nagoya City University Graduate School of Medical Sciences | Nagoya | Aichi-ken | Not Yet Recruiting |
| Ehime University | Tōon | Ehime | Not Yet Recruiting |
| University of Auckland | Auckland | Auckland | Not Yet Recruiting |
| Division of Cardiovascular & Pulmonary Diseases, Oslo University Hospital | Oslo | Oslo | Recruiting |
| Carol Davila University of Medicine and Pharmacy | Bucharest | Romania | Not Yet Recruiting |
| The Department of Cardiology at the Ljubljana University Medical Centre | Ljubljana | Slovenia | Not Yet Recruiting |
| Yonsei University College of Medicine | Seoul | Seoul | Not Yet Recruiting |
| Department of Cardiovascular Sciences, University of Birmingham | Birmingham | United Kingdom | Not Yet Recruiting |
| King's College | London | United Kingdom | Not Yet Recruiting |
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07436299 on ClinicalTrials.gov ↗ ← All trials in South Korea