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NCT07181291Completed

Pulsed Field or Cryoballoon Pulmonary Vein Isolation for Atrial Fibrillation in Heart Failure

Pulsed Field or Cryoballoon Pulmonary Vein Isolation for Atrial Fibrillation in Heart Failure (a Propensity Score Matched Comparison)

Source: ClinicalTrials.gov · Last updated 13 Feb 2026

Brief summary (registry, in English)

Patients with atrial fibrillation (AF) and heart failure with reduced left ventricular ejection fraction (HFrEF) are at particularly high cardiovascular risk. Rhythm-control by means of catheter-based pulmonary vein isolation (PVI) reduces all-cause mortality and rehospitalization for worsening heart failure in these patients. Considering the globally increasing use of the novel "pulsed-field ablation", it is necessary to determine whether this technique can be performed with the same safety and efficacy as the established cryoballoon ablation (CRYO) in this critically ill patient population. This retrospective, international, multicenter study compares the efficacy and safety of PFA versus CRYO in patients with AF and HFrEF (LVEF ≤40%) undergoing a first-time PVI-only procedure. Using propensity-score matching to minimize selection bias, the study will retrospectively evaluate whether a non-thermal PFA approach is non-inferior to the established thermal CRYO technique regarding rhythm control, while comparing procedural safety and efficiency in this high-risk population. Non-inferiority is tested against the assumption of a 12-month recurrence rate of 30% with a prespecified non-inferiority margin of 12% (corresponding to a hazard ratio of 1.53).

Status (registry)
Completed
Study type
Observational
Enrollment
700 (actual)
First submitted
11 Sept 2025
Start date
1 Sept 2025
Primary completion date
31 Dec 2025
Lead sponsor
St. Josefs-Hospital Wiesbaden GmbH
NCT number
NCT07181291

What you commit to

  • Study type: Observational
  • Participants enrolled: 700
  • From 1 Sept 2025 to the primary completion date, 31 Dec 2025
  • 12 sites in 2 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Lab values

  • Patients with LVEF \> 40%

Other

  • Patients who did not undergo pulsed field or cryoballoon ablation for first-time PVI
  • Patients who declined the use of their data during initial collection

Who the study is looking for

  • Patients with paroxysmal or persistent AF and echocardiographically confirmed HFrEF (LVEF ≤ 40%)
  • Patients who underwent their first PVI using pulsed field or cryoballoon ablation as part of clinical routine
  • Patients with regular follow-up via 12-lead ECG or Holter ECG following PVI
  • Patients with at least three months of follow-up

Age in the registry: 18 years to 99 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (12)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Montreal Heart Institute
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MontrealCanadaUnknown status
Vancouver General Hospital
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VancouverCanadaUnknown status
Kerckhoff Klinik, Bad Nauheim
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Bad NauheimGermanyUnknown status
Vivantes Klinikum am Urban
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BerlinGermanyUnknown status
Evangelisches Krankenhaus Düsseldorf
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DüsseldorfGermanyUnknown status
Universitätsklinikum Frankfurt am Main
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Frankfurt am MainGermanyUnknown status
Klinikum Fürth
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FürthGermanyUnknown status
Evangelisches Krankenhaus Hagen-Haspe
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HagenGermanyUnknown status
Universitätsklinikum Hamburg-Eppendorf
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Hamburg-EppendorfGermanyUnknown status
Medizinische Hochschule Hannover
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HanoverGermanyUnknown status
Universitätsklinikum Heidelberg
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HeidelbergGermanyUnknown status
St. Josefs Hospital Wiesbaden
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WiesbadenGermanyUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.