Marien Hospital Herne
Herne, North Rhine-Westphalia, Germany
NCT Number: NCT07783919
Comparison of single-shot PFA systems with focal dual-energy (PFA/RF) in patients at high risk of atrial fibrillation recurrence.
Trial opening soon.
Get Notified18 year and older
All sexes
Interventional
Not applicable
Herne, North Rhine-Westphalia, Germany
Catheter ablation via pulmonary vein isolation (PVI) is an established therapy for symptomatic paroxysmal and persistent atrial fibrillation. In recent years, pulsed-field ablation (PFA) has emerged as an innovative ablation technology. Unlike thermal ablation using radiofrequency or cryoablation, PFA relies on irreversible electroporation of the cell membrane, thereby enabling the selective ablation of cardiomyocytes while largely sparing adjacent structures such as the esophagus, phrenic nerve, and pulmonary veins. Clinical studies and registry data have demonstrated high efficacy and a favorable safety profile for PFA.
Various catheter systems are now available for performing PVI via PFA. These include single-shot systems, which facilitate rapid pulmonary vein isolation through a standardized and efficient workflow. Additionally, focal dual-energy catheters have been developed that combine pulsed-field ablation and radiofrequency ablation within a single catheter. These systems allow for tailored lesion delivery using electroanatomical mapping systems and may offer advantages, particularly in cases of complex anatomy or additional arrhythmogenic substrate.
Both single-shot and focal dual-energy systems have demonstrated high acute success rates and promising clinical outcomes in studies to date. However, there are currently no direct, prospective, randomized comparisons between the two ablation strategies. In particular, it remains unclear whether there are differences between the two approaches regarding long-term freedom from atrial arrhythmias, procedural efficiency, or safety.
Patients with persistent atrial fibrillation and those with a high comorbidity burden face an increased risk of atrial arrhythmia recurrence despite successful pulmonary vein isolation. While single-shot systems enable a standardized, rapid, and reproducible ablation procedure, focal dual-energy systems-due to their greater flexibility-may offer advantages in cases of complex anatomy and for individually tailored ablation strategies.
To date, there are no randomized clinical trials directly comparing these two ablation approaches. In particular, there is a lack of prospective data regarding patients at high risk for atrial arrhythmia recurrence. This study aims to bridge this evidence gap by investigating whether ablation using single-shot PFA is non-inferior to ablation using a focal dual-energy catheter in terms of clinical efficacy in patients at high risk of recurrence.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
CHA2DS2VA score ≥ 2, ≥ 1 cardioversion in the last 6 months or Left atrial (LA) diameter ≥ 45 mm
o or persistent atrial fibrillation (≥ 1 episode in the last 6 months)
Exclusion criteria
PFA-based Catheter Ablation for Atrial Fibrillation (PFA single shot vs. focal dual-eregy)
Time frame: 365 days, excluding the blanking period
Rate of participants with freedom from atrial arrhythmias (atrial fibrillation, atrial flutter, atrial tachycardia) during follow-up, excluding the blanking period
Time frame: 365 days, excluding the blanking period
Rate of participants with freedom from atrial fibrillation and rate of participants with freedom from atrial flutter or atrial tachycardia) during follow-up, excluding the blanking period
Time frame: Day of the ablation (periprocedural)
Rate of first-pass isolation of the pulmonary veins as well as rate of acute procedural success of the PVI
Time frame: Day of the procedure (periprocedural)
Total procedural time, fluoroscopy time, LA dwell time
Time frame: 365 days, excluding the blanking period
Correlation between procedural parameters (first-pass isolation rate, acute procedural success rate, total procedural time, fluoroscopy time) with clinical efficacy (rate of freedom from atrial arrhythmias (AF, AFL, AT)) during follow-up, excluding the blanking period
Time frame: day of the potential re-ablation (periprocedural)
In the event of a potential re-ablation, the rate of durable PVI will be assessed
Time frame: 365 days, excluding the blanking period
AFEQT questionnaire
Time frame: 365 days
Contact information is provided by the study sponsor or research team.
Marien Hospital Herne
Other
DUAL AF Single-Shot Versus Focal Dual-Energy Pulsed Field-Based Ablation for Atrial Fibrillation
Acronym: DUAL AF
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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