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Clinical Trials in the USA / NCT07800962
Enrolling by invitation Observational

Federated Learning for Point-of-Care Cardiac Ultrasound

NCT07800962 · tracked via the Priya Life Science USA tracker
Sponsor
Truway Health, Inc.
Phase
Observational
Started
2026-08-31
Last updated
2026-09-02

Condition(s) studied

Ventricular Dysfunction, LeftVentricular Function, LeftEchocardiographyUltrasonographyPoint-of-Care SystemsHeart Function TestsStroke VolumeFederated LearningMachine LearningArtificial Intelligence (AI)Deep LearningNeural Networks, ComputerImage Interpretation, Computer-AssistedDiagnosis, Computer-AssistedSensitivity and SpecificityROC Curve

Investigational drug(s) / intervention(s)

Focused Cardiac Point-of-Care UltrasonographyFL-POCUS Federated Machine-Learning Analysis System

Focused Cardiac Point-of-Care Ultrasonography: A clinically indicated, noninvasive focused cardiac ultrasound examination performed through a point-of-care ultrasound system. Standard views may include parasternal long-axis, parasternal short-axis, apical four-chamber, and subcostal views. The examination will be evaluated for image quality, cardiac-view classification, left ventricular function, and evidence of reduced left ventricular ejection fraction.

FL-POCUS Federated Machine-Learning Analysis System: Investigational software that analyzes focused cardiac point-of-care ultrasound examinations using a version-locked federated machine-learning model. The system evaluates cardiac-view classification, image quality, left ventricular function, and the probability of a left ventricular ejection fraction below 40%. During this observational validation study, all model outputs will remain in silent mode and will not influence clinical care. Raw ultrasound images and directly identifiable participant information will remain within each participating site's controlled environment.

Study summary

This prospective, multicenter study will evaluate a federated machine-learning system designed to analyze focused cardiac point-of-care ultrasound examinations. Federated learning allows participating clinical sites to contribute to model development while keeping raw ultrasound images and directly identifiable patient information within each site's controlled computing environment. Encrypted model updates, rather than patient images, will be transmitted for secure aggregation.

The prospective validation cohort will include approximately 3,000 adults undergoing clinically indicated focused cardiac ultrasound. Model performance will be compared with an expert interpretation of a comprehensive transthoracic echocardiogram performed within 24 hours. The primary objective is to determine how accurately the model identifies reduced left ventricular systolic function, defined as a left ventricular ejection fraction below 40%.

During the initial validation period, the investigational software will operate in silent mode. Its results will not be displayed to treating clinicians and will not be used to diagnose participants, select treatment, or replace standard clinical interpretation.

The study will also evaluate image-quality classification, cardiac-view recognition, performance across clinical sites and ultrasound systems, model calibration, processing time, cybersecurity, privacy resilience, and performance across demographic and clinical subgroups. Long-term monitoring will assess whether model performance changes as clinical populations, ultrasound equipment, acquisition practices, and software environments evolve during the 2026-2037 study period.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: * Age 18 years or older. * Undergoing a clinically indicated point-of-care cardiac ultrasound (POCUS) examination at a participating site. * Reference transthoracic echocardiogram completed within 24 hours of the index POCUS examination. * At least one cardiac ultrasound view attempted during the index examination. * POCUS and reference echocardiography records can be linked using an authorized coded study identifier. * Participant consent obtained or inclusion authorized under an Institutional Review Board-approved consent waiver, as applicable. Exclusion Criteria: * Reference transthoracic echocardiogram not completed within 24 hours of the index POCUS examination. * Major cardiac procedure or substantial hemodynamic intervention occurring between the POCUS examination and reference echocardiogram, including cardiac surgery, cardioversion, cardiac arrest, or initiation of mechanical circulatory support. * Ultrasound or reference data are missing, corrupted, irretrievable, or cannot be securely linked. * Previous inclusion of the same participant in the primary validation cohort, unless repeat examinations are authorized under a prespecified longitudinal analysis. * Declines participation when individual informed consent is required. * Member of a population not authorized for enrollment under the applicable Institutional Review Board approval.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Truway Health, Inc. New York New York

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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 NCT07800962 on ClinicalTrials.gov ↗ ← All trials in the USA