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Atrial Fibrillation (AF)DUAL AFNCT07783919

Single-Shot Versus Focal Dual-Energy Pulsed Field-Based Ablation for Atrial Fibrillation

A study testing Catheter Ablation for Atrial Fibrillation in people with Atrial Fibrillation (AF), run by Marien Hospital Herne at 1 site in Germany.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

Comparison of single-shot PFA systems with focal dual-energy (PFA/RF) in patients at high risk of atrial fibrillation recurrence. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Atrial Fibrillation (AF)
What is being tested?
Catheter Ablation for Atrial Fibrillation
Type of treatment
Surgery or procedure
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
268 participants
Where
1 siteGermany
Study dates
1 Sep 2026to 31 Dec 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Age ≥ 18 years
  • First-time pulmonary vein isolation
  • Symptomatic atrial fibrillation:
  • Paroxysmal atrial fibrillation (≥ 2 episodes in the last 6 months) and one of the following:
  • 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)

Who cannot join

  • Atrial fibrillation due to reversible or non-cardiac causes
  • Severe mitral or tricuspid valve regurgitation requiring therapy
  • Previous left atrial endocardial or epicardial ablation
  • Pregnancy or breastfeeding
  • Lack of opportunity for reliable study participation

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Dimitrios Bismpos, Dr.med. contact

+49023234995609

Dimitrios.Bismpos@elisabethgruppe.de

Germany1 site
  • Marien Hospital Herne

    Herne, North Rhine-Westphalia

    Dimitrios Bismpos, +49023234995609, Dimitrios.Bismpos@elisabethgruppe.de

Other trials in Germany

About this study

Official title: DUAL AF Single-Shot Versus Focal Dual-Energy Pulsed Field-Based Ablation for Atrial Fibrillation

Comparison of single-shot PFA systems with focal dual-energy (PFA/RF) in patients at high risk of atrial fibrillation recurrence.

Read the detailed description

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.

Being tested
Catheter Ablation for Atrial Fibrillation
Medical subject headings
Atrial Fibrillation

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Catheter Ablation for Atrial FibrillationProcedure or surgery

    PFA-based Catheter Ablation for Atrial Fibrillation (PFA single shot vs. focal dual-eregy)

Study groups in NCT07783919
Study groupRoleWhat they receive
Single shot PFA-based Ablation for AFActive comparatorNot described
Receives: Procedure: Catheter Ablation for Atrial Fibrillation
Focal Dual-Energy-based Ablation for Atrial FibrillationPlacebo comparatorNot described
Receives: Procedure: Catheter Ablation for Atrial Fibrillation

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Freedom from atrial arrhythmias during follow-up

    Rate of participants with freedom from atrial arrhythmias (atrial fibrillation, atrial flutter, atrial tachycardia) during follow-up, excluding the blanking period

    Measured: 365 days, excluding the blanking period

Secondary outcomes (7)
  1. Freedom from atrial fibrillation/atrial tachycardia

    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

    Measured: 365 days, excluding the blanking period

  2. First-pass isolation rate and acute PVI success

    Rate of first-pass isolation of the pulmonary veins as well as rate of acute procedural success of the PVI

    Measured: Day of the ablation (periprocedural)

  3. Procedural durations

    Total procedural time, fluoroscopy time, LA dwell time

    Measured: Day of the procedure (periprocedural)

  4. Correlation between procedural parameters and clinical efficacy

    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

    Measured: 365 days, excluding the blanking period

  5. Electroanatomical evaluation in the event of potential re-ablation

    In the event of a potential re-ablation, the rate of durable PVI will be assessed

    Measured: day of the potential re-ablation (periprocedural)

  6. Patient-reported outcome measures (PROMs)

    AFEQT questionnaire

    Measured: 365 days, excluding the blanking period

  7. Occurrence of serious adverse events

    Measured: 365 days

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted25 Aug 2026
  2. Study start1 Sep 2026 (estimated)
  3. Primary completion31 Aug 2027 (estimated)
  4. Study completion31 Dec 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Participant
Enrolment
268 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07783919
Sponsor's protocol ID
DUAL-AF-2026-01
Acronym
DUAL AF
Status last verified
Aug 2026
First submitted
13 Aug 2026
Last updated
25 Aug 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A study testing Catheter Ablation for Atrial Fibrillation in people with Atrial Fibrillation (AF), run by Marien Hospital Herne at 1 site in Germany.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 25 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Germany. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Dimitrios Bismpos, Dr.med. (+49023234995609, Dimitrios.Bismpos@elisabethgruppe.de), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Freedom from atrial arrhythmias during follow-up (time frame: 365 days, excluding the blanking period). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 25 Aug 2026.

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