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AI-Enabled Direct-from-ECG Ejection Fraction (EF) Severity Assessment Using COR ECG Wearable Monitor

Study acronym: EFACT
StatusRecruiting
PhaseNot specified
Started2024-11-21
View on ClinicalTrials.gov ↗
This prospective, multicenter, cluster-randomized controlled study aims to evaluate the accuracy of an investigational artificial intelligence (AI) Software as a Medical Device (SaMD) designed to compute ejection fraction (EF) severity categories based on the American Society of Echocardiography's (ASE) 4-category scale. The software analyzes continuous ECG waveform data acquired by the FDA-cleared Peerbridge COR® ECG Wearable Monitor, an ambulatory patch device designed for use during daily activities. The AI software assists clinicians in cardiac evaluations by estimating EF severity, which reflects how well the heart pumps blood. In this study, EF severity determination will be made using 5-minute ECG recordings collected during a 15-minute resting period with participants seated upright. The results will be compared to EF severity obtained from an FDA-cleared, non-contrast transthoracic echocardiogram (TTE) predicate device. This comparison aims to validate the accuracy of the AI software.

Amendment record

Amended 4 times since 2024-11-18; most recent filed 2026-05-28. Every amendment is listed below.

Dates here are the day the sponsor filed the amendment, not the day ClinicalTrials.gov published it. Version history last read from ClinicalTrials.gov on 2026-08-30.

2026-05-28
Amendment Study Status, Study Design, Arms and Interventions, Contacts/Locations, IPDSharing v4
2025-02-09
Amendment Study Status, Conditions, Contacts/Locations v3
2024-12-17
Amendment Enrolling by InvitationRecruiting Study Status, Contacts/Locations v2
2024-11-20
Amendment Study Identification, Study Status, Study Description, Conditions v1
2024-11-18
Original filing
Trial Details
NCT Number NCT06699056
Lead Sponsor Peerbridge Health, Inc
Conditions Ventricular Ejection Fraction, LVF, LV Dysfunction, Atrial Enlargement, Conduction Defect, Heart Failure, Valvular Heart Disease, Ischemic Heart Disease +7 more
Enrollment 2,000 participants
Start Date 2024-11-21
Primary Completion 2027-11-15 (estimated)
Study Completion 2027-11-15 (estimated)
Updated on ClinicalTrials.gov 2026-06-01