CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 85 enrolled
Drug / intervention
Electrographic Flow™ guided 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/NCT04473963
NCT04473963N/ACompleted

A Randomized Controlled Study to Evaluate the Reliability of Electrographic Flow™ (EGF) Mapping Algorithm Technology to Identify Sources of Atrial Fibrillation and Guide Ablation Therapy in Patients With Persistent Atrial Fibrillation

Cortex·interventional·Posted Jul 16, 2020·Updated Apr 10, 2025

In Brief

A clinical study evaluating Electrographic Flow™ guided ablation for Atrial Fibrillation, Persistent. Completed, enrolled 85 participants across 4 sites in 3 countries.

Detailed Summary

This study is to evaluate Electrographic Flow™ (EGF) mapping algorithm technology (Ablamap® Software).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesCzechia, Germany, Netherlands
CollaboratorsAblacon, Inc.

Timeline

N/ACompletedFinished
2020202120222023202420252026
First PostedJul 16, 2020
Enrollment StartSep 27, 2019
Primary CompletionSep 27, 2021
TodayJul 2, 2026
Enrollment to primary: 2 yearsPosted 6.0 years ago

Interventions

Electrographic Flow™ guided ablationdevice

In addition to standard pulmonary vein isolation (PVI) or PVI touch-up, subjects receive targeted radiofrequency source ablation guided by Electrographic Flow™ (EGF) mapping. 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 software. Several basket catheter positions are acquired in standard positions in both the left and right atria. EGF-identified sources with activity above the threshold (≥ 26.5%) are considered significant and targeted for ablation. The procedure concludes when all EGF-identified sources are eliminated, defined as reducing source activity below the threshold.