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Recruiting NCT07018596

NS-PFA Catheter Ablation of Paroxysmal Atrial Fibrillation With the Pulse Biosciences CellFX System

No phase Interventional Atrial Fibrillation Paroxysmal Cardiac Ablation Cardiac Arrhythmia

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: CellFX nsPFA Cardiac Catheter System.
Who it may be relevant to
Registry conditions: Atrial Fibrillation Paroxysmal, Cardiac Ablation, Cardiac Arrhythmia. Basic parameters: 18 years — 85 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Czechia
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Safety and Effectiveness of the CellFX® nsPFA Catheter Endocardial Ablation System for the Treatment of Paroxysmal Atrial Fibrillation

Overview

The objective of this study is to demonstrate the safety and effectiveness of the CellFX nano-second Pulsed Field Ablation (nsPFA) Cardiac Catheter Ablation System in treating recurrent, drug-resistant, symptomatic paroxysmal atrial fibrillation (AF).

Detailed description

This study is a prospective, multicenter, non-randomized clinical investigation. Eligible participants with drug-resistant paroxysmal AF who are clinically indicated for a cardiac catheter ablation procedure will undergo nsPFA ablation with the CellFX Cardiac Catheter Ablation System. The primary endpoints will be assessed at 6 months after the ablation procedure.

Interventions

  • Device CellFX nsPFA Cardiac Catheter System
    The CellFX nsPFA Cardiac Catheter System includes the nsPFA 360 Endocardial Ablation Catheter, CellFX Console, switcher box/adapter, and sensing cable. The System is a proprietary endocardial catheter system designed for use in cardiac electrophysiology procedures to treat arrhythmias, including atrial fibrillation. The nano-PFA 360 Catheter ablates cardiac tissue using nonthermal nanosecond pulses of electrical energy. nsPFA is a cell-specific, nonthermal ablation technology that delivers nanos

Primary outcome measures

  • Proportion of participants with freedom from primary safety endpoint [Time frame: Within 7 days, 30 days, and 6 months post-ablation procedure]
  • Proportion of participants achieving freedom from treatment failure. [Time frame: 6 months post-ablation]
Secondary outcome measures (1)
  • Proportion of participants achieving acute procedural success [Time frame: Immediately post-ablation procedure]

Eligibility criteria

Inclusion criteria

  • A diagnosis of recurrent drug-resistant symptomatic paroxysmal AF defined as AF that terminates spontaneously or with intervention within seven (7) days of onset, documented by the following:

i. Physician's note indicating the presence of AF symptoms and at least two (2) episodes of self-terminating AF within six (6) months prior to enrollment

  • Age 18 through 85 years old (or older than 18 if required by local law)
  • Failure of at least one AAD (class I or III) for AF as evidenced by recurrence of symptomatic AF, or intolerable side effects due to AAD.
  • Participant is willing and capable of providing Informed Consent
  • Received a standard cardiac work up and is an appropriate candidate for an investigational procedure as determined by study investigators

Exclusion criteria

  • Left atrial diameter ≥5.5 cm (anteroposterior)
  • Any of the following within 3 months prior to enrollment:
  • Any cardiac surgery
  • Myocardial infarction
  • Percutaneous Coronary Intervention (PCI) / Percutaneous Coronary Intervention (PTCA) or coronary artery stenting
  • Unstable angina
  • Pericarditis or symptomatic pericardial effusion
  • Any of the following within 6 months prior to enrollment:
  • Any cerebral ischemic event (stroke or transient ischemic attack (TIA)
  • History of thromboembolic event
  • Prior history of medical procedure involving instrumentation of the left atrium (previous ablation, atrial septal defect (ASD) closure, Left atrial appendage occlusion)
  • Planned Left Atrial Appendage (LAA) closure procedure, Transcatheter Aortic Valve Replacement (TAVR), Mitraclip, Atrial Septal Defect (ASD) or Patent Foramen Ovale (PFO) closure, Triclip or implant of an Implantable Loop Recorder (ILR), permanent pacemaker, biventricular pacemaker, or any implantable cardiac defibrillator (with or without biventricular pacing function) during or for any time during the follow-up period
  • Patient who is not on oral anticoagulation therapy for at least 3 weeks prior to the ablation procedure
  • Documented left atrial (LA) thrombus by imaging within 48 hours of the procedure.
  • Presence of a permanent pacemaker, biventricular pacemaker, or any type of implantable cardiac defibrillator (with or without biventricular pacing function).
  • Prior diagnosis of pulmonary vein stenosis
  • Valvular cardiac surgical/percutaneous procedure (e.g., ventriculotomy, atriotomy, and valve repair or replacement and presence of a prosthetic valve).
  • Moderate to severe mitral valve stenosis
  • More than moderate mitral regurgitation (i.e., 3+ or 4+ MR)
  • New York Heart Association (NYHA) Class III or IV congestive heart failure or documented left ventricular ejection fraction (LVEF) less than or equal to 35% measured by acceptable cardiac testing (e.g., TTE)
  • History of pulmonary hypertension with pulmonary systolic artery pressure >50 mm Hg, severe Chronic Obstructive Pulmonary Disease or restrictive lung disease
  • Rheumatic heart disease
  • Contraindication to anticoagulation (i.e., Heparin, Dabigatran, Apixaban, Vitamin K Antagonists such as warfarin)
  • Active systemic infection
  • Hypertrophic or advanced infiltrative cardiomyopathy
  • Atrial myxoma
  • Known reversible causes of AF, including but not limited to uncontrolled hyperthyroidism, severe untreated obstructive sleep apnea, and acute alcohol toxicity
  • History of abnormal bleeding and/or clotting disorder
  • Renal insufficiency with an estimated glomerular filtration rate (eGFR) < 30 mL/min/1.73 m2, or any history of renal dialysis or renal transplant
  • History of severe chronic gastrointestinal problems involving the esophagus, stomach and/or untreated acid reflux
  • Solid organ or hematologic transplant, or currently being evaluated for an organ transplant
  • Any woman known to be pregnant or breastfeeding, or any woman of childbearing potential who is not on a reliable form of birth regulation method or abstinence
  • Other criteria, which the Investigator determines would make the patient unsuitable to participate (e.g. uncontrolled drug and/or alcohol addiction, congenital disease, fragility)
  • Body Mass Index (BMI) > 40.0
  • Participants with any other significant uncontrolled or unstable medical condition (such as uncontrolled brady-arrhythmias, ventricular arrhythmias, hyperthyroidism or significant coagulation disorder)
  • Life expectancy less than one year
  • Current or anticipated participation in any other clinical study of a drug, device, or biologic during the duration of the study not pre-approved by the Sponsor
  • Unwilling or unable to comply fully with study procedures and follow-up

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Treatment

Study locations

Czechia · 1 center
  • Na Homolce Hospital — Prague

Identifiers

NCT: NCT07018596 · NP-CCP-US-043

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗