CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 25 enrolled
Drug / intervention
Electrographic Flow™ (EGF) mapping and ablationdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT05481359
NCT05481359N/ACompleted

A Post Market, Global Registry to Evaluate the Identification of Atrial Fibrillation Sources Using Electrographic Flow (EGF™) Mapping System to Guide Ablation Therapy in Patients With Atrial Fibrillation in Real-world Setting.

Ablacon, Inc.·observational·Posted Aug 1, 2022·Updated Apr 10, 2025

In Brief

An observational study evaluating Electrographic Flow™ (EGF) mapping and ablation for Atrial Fibrillation, Persistent and 3 related conditions. Completed, enrolled 25 participants across 5 sites in 3 countries.

Detailed Summary

This post-market global registry will evaluate the ability of Electrographic Flow (EGF™) mapping to identify atrial fibrillation (AF) sources and guide ablation therapy in patients with atrial fibrillation in real-world setting.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesNetherlands, Poland, United States
CollaboratorsCortex

Timeline

N/ACompletedFinished
2023202420252026
First PostedAug 1, 2022
Enrollment StartSep 12, 2022
Primary CompletionOct 27, 2022
Study CompletionNov 17, 2023
TodayJul 2, 2026
Enrollment to primary: 2 monthsPosted 3.9 years ago

Interventions

Electrographic Flow™ (EGF) mapping and ablationdevice

Electrographic Flow™ (EGF) mapping enables the full spatiotemporal reconstruction of organized atrial electrical wavefront propagation to identify active sources or origins of excitation that may trigger atrial fibrillation (AF). EGF mapping involves 1 minute recordings of unipolar electrograms from a basket catheter, which are then processed with the EGF algorithm (Ablamap® Software). Several basket catheter positions are acquired in standard positions in both the left and right atria. EGF-identified sources with activity levels exceeding the recommended threshold are deemed significant and are targeted for ablation. The success of the ablation is confirmed through an EGF remap, where elimination of the source is defined as reduction of EGF source activity below the threshold.