RECRUITINGINTERVENTIONAL

Comparison of Different Pulsed Field Ablation Catheters in Atrial Fibrillation

Comparison of Different Pulsed Field Ablation Catheters Combined With Stroke Prevention in High Stroke Risk·Atrial Fibrillation: A Prospective, Multicenter, Randomized Controlled Trial

About This Trial

Pulsed field energy ablation, a non-thermal ablation modality, can potentially reduce post-ablation tissue edema. Previous studies have confirmed the feasibility and safety of combined pulsed field ablation (PFA) and left atrial appendage closure (LAAC) as a one-stop treatment, with few reports of post-ablation tissue edema. However, during PFA procedures, the presence of metallic components in the ablation site (e.g., occluder frames, metallic valves) may lead to arcing during energy delivery, compromising procedural safety. Therefore, when performing PFA+LAAC as a one-stop procedure, a "ablation-first" strategy is recommended. Due to the influence of parameters such as voltage, pulse width, and number of cycles on pulsed field energy characteristics, significant variability in ablation depth and area may exist between different PFA devices. To date, no large-scale clinical studies have compared the efficacy and safety of different PFA systems. Accordingly, this study will conduct a prospective, multicenter, randomized controlled trial to compare the effectiveness and safety of domestic versus imported pulsed field ablation catheters in the treatment of patients with atrial fibrillation.

Who May Be Eligible (Plain English)

Who May Qualify: 1. Older than 18 years. 2. Diagnosed with drug-refractory, symptomatic atrial fibrillation. 3. The patient has a high risk of stroke (CHA2DS2-VA score ≥ 2). 4. Have a situation of: 1. requires oral anticoagulation therapy 2. high bleeding risk (HAS-BLED score ≥ 3) that unsuitable for or unwilling to undergo long-term oral anticoagulation therapy. 5. Subjects are able to understand the purpose of the study, voluntarily participate in the study and sign the willing to sign a consent form, and are willing to complete the follow-up according to the requirements of the program. Who Should NOT Join This Trial: 1. History of persistent atrial fibrillation \>1 year. 2. Atrial fibrillation was secondary to thyroid disease or other reversible reasons. 3. Left atrial anteroposterior diameter \>50 mm. 4. Evidence of left atrial or left atrial appendage thrombus on imaging examination. 5. Concurrent other arrhythmias required for catheter ablation (e.g., atrioventricular reentrant tachycardia, atrioventricular nodal reentrant tachycardia, pre-excitation syndrome) prior to enrollment. 6. Rheumatic heart disease. 7. Left ventricular ejection fraction \<40% or New York Heart Association (NYHA) class III/IV. 8. Unstable angina. 9. Myocardial infarction (MI), coronary artery bypass grafting (CABG), or percutaneous coronary intervention (PCI) within 3 months prior to enrollment. 10. History of prior left atrial appendage closure, patent foramen ovale closure, atrial septal defect closure, or repair surgery. 11. Implantation of a mechanical mitral valve prosthesis or metallic annuloplasty rings. 12. Presence of intracardiac thrombus, space-occupying lesions, or other abnormalities that preclude vascular access or catheter manipulation. 13. Contraindications to anticoagulation or history of coagulation disorders/abnormal bleeding. 14. Active systemic infection. 15. Estimated glomerular filtration rate (eGFR) \<30 mL/min/1.73 m² or history of renal dialysis. ...See full criteria on ClinicalTrials.gov Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language

Inclusion Criteria: 1. Older than 18 years. 2. Diagnosed with drug-refractory, symptomatic atrial fibrillation. 3. The patient has a high risk of stroke (CHA2DS2-VA score ≥ 2). 4. Have a situation of: 1. requires oral anticoagulation therapy 2. high bleeding risk (HAS-BLED score ≥ 3) that unsuitable for or unwilling to undergo long-term oral anticoagulation therapy. 5. Subjects are able to understand the purpose of the study, voluntarily participate in the study and sign the informed consent, and are willing to complete the follow-up according to the requirements of the program. Exclusion Criteria: 1. History of persistent atrial fibrillation \>1 year. 2. Atrial fibrillation was secondary to thyroid disease or other reversible reasons. 3. Left atrial anteroposterior diameter \>50 mm. 4. Evidence of left atrial or left atrial appendage thrombus on imaging examination. 5. Concurrent other arrhythmias required for catheter ablation (e.g., atrioventricular reentrant tachycardia, atrioventricular nodal reentrant tachycardia, pre-excitation syndrome) prior to enrollment. 6. Rheumatic heart disease. 7. Left ventricular ejection fraction \<40% or New York Heart Association (NYHA) class III/IV. 8. Unstable angina. 9. Myocardial infarction (MI), coronary artery bypass grafting (CABG), or percutaneous coronary intervention (PCI) within 3 months prior to enrollment. 10. History of prior left atrial appendage closure, patent foramen ovale closure, atrial septal defect closure, or repair surgery. 11. Implantation of a mechanical mitral valve prosthesis or metallic annuloplasty rings. 12. Presence of intracardiac thrombus, space-occupying lesions, or other abnormalities that preclude vascular access or catheter manipulation. 13. Contraindications to anticoagulation or history of coagulation disorders/abnormal bleeding. 14. Active systemic infection. 15. Estimated glomerular filtration rate (eGFR) \<30 mL/min/1.73 m² or history of renal dialysis. 16. Pregnancy or breastfeeding. 17. Life expectancy \<12 months (e.g., advanced malignancy). 18. Current or anticipated participation in other drug or device clinical trials. 19. Any other condition or abnormality deemed by the investigator to warrant exclusion.

Treatments Being Tested

DEVICE

CardiPulse

abc

DEVICE

FaraPulse

bcd

Locations (1)

Ningbo First Hospital

Hangzhou, China