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.
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.
Germany1 site
Marien Hospital Herne
Herne, North Rhine-Westphalia
Dimitrios Bismpos, +49023234995609, Dimitrios.Bismpos@elisabethgruppe.de
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.
- Conditions
- Atrial Fibrillation (AF)
- 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 group | Role | What they receive |
|---|---|---|
| Single shot PFA-based Ablation for AF | Active comparator | Not described Receives: Procedure: Catheter Ablation for Atrial Fibrillation |
| Focal Dual-Energy-based Ablation for Atrial Fibrillation | Placebo comparator | Not 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.
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)
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
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)
Procedural durations
Total procedural time, fluoroscopy time, LA dwell time
Measured: Day of the procedure (periprocedural)
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
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)
Patient-reported outcome measures (PROMs)
AFEQT questionnaire
Measured: 365 days, excluding the blanking period
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.
- First posted25 Aug 2026
- Study start1 Sep 2026 (estimated)
- Primary completion31 Aug 2027 (estimated)
- Study completion31 Dec 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Atrial Fibrillation (AF)Studies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Marien Hospital Herne
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Dimitrios Bismpos, Marien Hospital Herne
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
Study at a glance
From the registry record, last updated by the sponsor on 25 Aug 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- DUAL AF Single-Shot Versus Focal Dual-Energy Pulsed Field-Based Ablation for Atrial Fibrillation
- ClinicalTrials.gov ID
- NCT07783919
- Acronym / sponsor ID
- DUAL AF / DUAL-AF-2026-01
- Conditions
- Atrial Fibrillation (AF)
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 268 participants (estimated)
- Lead sponsor
- Marien Hospital HerneUniversity, hospital or other
- Study start
- 1 Sep 2026 (estimated)
- Primary completion
- 31 Aug 2027 (estimated)
- Study completion
- 31 Dec 2027 (estimated)
- First posted
- 25 Aug 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Comparison of single-shot PFA systems with focal dual-energy (PFA/RF) in patients at high risk of atrial fibrillation recurrence.
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.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (participant)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Single shot PFA-based Ablation for AF | Active comparator | Procedure: Catheter Ablation for Atrial Fibrillation |
| Focal Dual-Energy-based Ablation for Atrial Fibrillation | Placebo comparator | Procedure: Catheter Ablation for Atrial Fibrillation |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (6 listed)
- Age ≥ 18 years
- First-time pulmonary vein isolation
- Symptomatic atrial fibrillation:
- 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)
Key exclusion criteria (5 listed)
- 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
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Catheter Ablation for Atrial FibrillationPFA-based Catheter Ablation for Atrial Fibrillation (PFA single shot vs. focal dual-eregy) | Procedure or surgery | Focal Dual-Energy-based Ablation for Atrial Fibrillation, Single shot PFA-based Ablation for AF |
Primary outcome
Freedom from atrial arrhythmias during follow-up
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
7 secondary outcomes
Freedom from atrial fibrillation/atrial tachycardia
Time frame: 365 days, excluding the blanking period
First-pass isolation rate and acute PVI success
Time frame: Day of the ablation (periprocedural)
Procedural durations
Time frame: Day of the procedure (periprocedural)
Correlation between procedural parameters and clinical efficacy
Time frame: 365 days, excluding the blanking period
Electroanatomical evaluation in the event of potential re-ablation
Time frame: day of the potential re-ablation (periprocedural)
Patient-reported outcome measures (PROMs)
Time frame: 365 days, excluding the blanking period
Occurrence of serious adverse events
Time frame: 365 days
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 25 Aug 2026.
- Individual participant dataSharing planned: Undecided
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ATRIAL APPENDAGE CLOSURE for ATRIAL FIBRILLATION, Atrial Fibrillation (AF)
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
1 site in 1 country: see every site and its status.
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.