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By invitation only Not applicable NCT07137455

EDEN Intracardiac Electrogram Recording and Classifying System

No applicable phase (e.g. observational)
Conditions: Ventricular Arrhythmia

Sponsor: National Heart, Lung, and Blood Institute (NHLBI)

trial.available_in: БГ
Overview
Background: Heart surgeons use electrocardiogram (ECG) machines to record electrical signals from the heart during procedures. Normal ECG machines connect only to the skin. Special ECG machines connect directly to the heart; they are a safer option during procedures. Researchers want to test a new ECG machine called the EDEN system. Objective: To test the EDEN system in people having heart procedures. The new system will be used along with an approved special ECG machine. Eligibility: People aged 21 years or older who need to have a heart procedure. These procedures can include (1) electrophysiology mapping or ablation; and (2) conduction system pacing. Design: Researchers will review participants' medical records. No extra tests are needed. Participants will have their heart procedure as planned. The EDEN system will be linked to the special ECG used during the procedure. An extra electrode may be placed on the participant's body. Electrodes are small stickers attached to wires that go to the machine. The EDEN system will record and analyze electrical signals already being measured. It will not interfere with participants' care. No medical decisions well be made based on its data. No follow-up visits are needed for this study....
Description
Study Description: The study tests a hardware electrocardiography appliance used to record and classify intracardiac electrograms obtained in the practice of medicine. No diagnoses or clinical decisions are based on the findings in this study. Objectives: The primary objective is to determine whether the classifier accurately identifies the EDEN radial depth category. Endpoints: Primary endpoint: The primary endpoint is classifier accuracy. Exploratory endpoints: Correspondence of EDEN electrograms with CT and CMR findings (of myocardial segmental thickness, scar, and possibly relaxometry); Impact of abnormal conduction, induced or observed during the EP procedure, on EDEN electrogram morphology. Technical success of acquiring and classifying EDEN electrograms.
Who can participate
* INCLUSION CRITERIA * Age \>= 21 years * Undergoing a medically-necessary invasive cardiac electrophysiology mapping and/or ablation procedure for ventricular arrhythmia, or conduction system pacing procedure EXCLUSION CRITERIA * Does not consent to participate, or unable to consent to participate * Hemodynamic instability or emergency procedure
Interventions
EDEN Intracardiac Electrogram Recording and Classifying System
DEVICE
Locations 1
United States (1)
Emory University Hospital
Atlanta , Georgia
Technical details
Status
By invitation only
Phase
Not applicable
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
21 Years
Maximum age
100 Years
Healthy volunteers
No
Start date
29.04.2026
Completion date
01.11.2026
Registry ID
NCT07137455
Source
clinicaltrials.gov
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