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Clinical Trials in South Korea / NCT06811519
Recruiting Observational

AI-based Prediction of Cardiac Function Using Echocardiography and Body Composition Data (ECHO-FIT Study)

NCT06811519 · tracked via the Priya Life Science South Korea tracker
Phase
Observational
Started
2025-02-24
Last updated
2025-03-04

Condition(s) studied

Heart FailureLeft Ventricular (LV) Systolic DysfunctionBody Composition MeasurementArtificial Intelligence (AI)

Investigational drug(s) / intervention(s)

Body Composition Analyzer (ACCUNIQ BC720)

Body Composition Analyzer (ACCUNIQ BC720): Body Composition Analyzer (ACCUNIQ BC720)

Study summary

This prospective observational study (ECHO-FIT Study) aims to develop and validate a predictive model for cardiac function, particularly left ventricular ejection fraction (LVEF), by integrating echocardiographic measurements with body composition data obtained from the QCCUNIQ BC 720 device.

The study plans to enroll 2,000 adult participants, comprising 1,000 individuals with normal LVEF (≥50%) and 1,000 with heart failure (LVEF \<50%), all of whom will undergo standard-of-care echocardiography and body composition analysis.

By analyzing the relationships between key echocardiographic parameters (such as LVEF and diastolic function) and body composition measures (including fat mass, skeletal muscle mass, and total body water), we will develop a non-invasive prediction model capable of identifying individuals at higher risk of cardiac dysfunction.

This innovative approach has the potential to enhance early detection and personalized management of heart failure, reduce dependence on resource-intensive diagnostic procedures, and ultimately improve patient outcomes.

Eligibility

Sex
ALL
Min age
20 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * Aged 20 years or older. * Undergoing a standard echocardiographic examination. * Providing consent to undergo body composition analysis. * Signing the informed consent form to voluntarily participate in the study. Exclusion Criteria: * Having a physical or mental condition that makes it impossible to conduct an echocardiogram or perform body composition analysis. * Deemed inappropriate for study participation by the researcher (e.g., unable to cooperate).

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Yongin Severance Hospital Yongin Gyeonggi-do Recruiting

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Official registry record

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 NCT06811519 on ClinicalTrials.gov ↗ ← All trials in South Korea