Versatility of a Circular Multielectrode Catheter in the Individualized Recognition & Treatment of Atrial Fibrillation and Related Arrhythmias Using Pulsed Field Energy

Atrial Fibrillation and Flutter Clinical Trial

— VIRTUE  

Official title:

Versatility of a Circular Multielectrode Catheter in the Individualized Recognition & Treatment of Atrial Fibrillation and Related Arrhythmias Using Pulsed Field Energy

Clinical Trial Details — Status: Enrolling by invitation

Administrative data

• NCT number: NCT06056557
• Other study ID #: STUDY-23-00978
• Status: Enrolling by invitation
• Phase: N/A
• Start date: September 28, 2023
• Est. completion date: December 31, 2024

Study information

• Verified date: October 2023
• Source: Icahn School of Medicine at Mount Sinai
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this pragmatic study is to evaluate the safety, performance and effectiveness of the VARIPULSE catheter technology used in combination with the TRUPULSE™ Generator, and the compatible EAM system (Carto 3D) to treat patients with atrial fibrillation and related arrhythmias during clinically-indicated ablation procedures.

Description:

By virtue of its efficiency, safety profile, and potential for improved efficacy in certain patient populations (e.g., thickened atrial tissue of hypertrophic cardiomyopathy (HCM) patients), there is tremendous excitement about the role of pulsed field ablation (PFA) to treat atrial fibrillation and related arrhythmias. However, most PFA clinical trials enroll very selected populations and have highly focused inclusion/exclusion criteria - for example, typically only paroxysmal or persistent atrial fibrillation (AF) patients with upper age criteria are included, other disease states such as HCM are excluded, and typically redo ablation procedures are also excluded. The latter is particularly problematic since redo procedures are quite prevalent in most physicians' clinical practice. In some sense, the incorporation of these restrictive criteria is not terribly surprising since most of the novel PFA catheters are specifically designed to perform only certain aspects of the AF ablation procedure (e.g., just PVI). That is, when there are more complex substrates (where other types of lesion sets may be needed), it may not be practical to allow a more inclusive criteria for enrollment. Of course, the downside is that the majority of the patients that are eventually treated in clinical practice are not reflected by the enrolled patient population. The VARIPULSE™ catheter technology is a novel circular catheter with a variable loop design, containing multiple electrodes with individual irrigation pores capable of delivering pulse-field energy. The Ablation procedure will follow the below sequence: - Anatomical and voltage mapping of the left and/or right atrium - To perform this mapping, the VARIPULSE bi-directional catheter or a compatible conventional FDA-approved multi-electrode mapping catheter (e.g., Pentaray, Octaray or Optrell) may be used - Activation mapping of any-presenting or inducible atrial flutter - Pulmonary Vein Isolation (PVI) to be achieved in all patients with atrial fibrillation (if not already achieved). - Confirmation of entrance block with adenosine or isoproterenol challenge - Additional ablation lesion sets are per the investigator's discretion including: - Posterior wall Isolation - Regional fractionation clusters - Cavo-tricuspid isthmus Line - Mitral Isthmus Line - Any micro-/macro-reentrant atrial tachycardia's - As part of the ablation procedure, any safety assessments that are considered important (e.g., EGD, coronary angiography, etc.) may be performed; these data will also be collected. This study is a prospective, single-center, non-randomized, interventional clinical study to determine the safety and efficacy in using BWI IRE ablation system in a variety of atrial arrhythmias. Subjects will be followed for 12 months post-procedure.

Recruitment information / eligibility

• Status: Enrolling by invitation
• Enrollment: 150
• Est. completion date: December 31, 2024
• Est. primary completion date: December 31, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Age 18 or older.
• Diagnosed with atrial fibrillation or atrial atypical atrial flutter (typical flutter may also be ablated provided that the typical flutter occurs in addition to atrial fibrillation or atypical flutter; that is, typical flutter as the sole arrhythmia should not undergo PFA).
• Previous surgical or catheter ablation for atrial fibrillation is allowed
• Planned for a catheter ablation procedure
• Able and willing to provide written consent and comply with all testing and follow-up requirements
• Have in place or are planned to receive an implantable loop recorder, pacemaker or defibrillator capable of recording atrial rhythm

Exclusion Criteria:

• Documented "active" left atrial thrombus
• Conditions that preclude the introduction and manipulation of intracardiac catheters:

eg, active intracardiac thrombus, myxoma, tumor, a prohibitive interatrial baffle or patch, etc.)

• Previous PCI/MI within the past 1 month
• Active systemic infection or sepsis
• Uncontrolled heart failure - New York Heart Association (NYHA) function class IV.
• History of blood clotting, bleeding abnormalities or contraindication to anticoagulation.
• Significant congenital anomaly or medical problem that in the opinion of the investigator would preclude enrollment.
• Women who are pregnant, lactating, or who are of childbearing age and plan on becoming pregnant during this trial.
• Life expectancy or other disease processes likely to limit survival to less than 12 months.
• Currently enrolled in an investigational study evaluating another device, biologic, or drug, that would interfere with this trial.

Related Conditions & MeSH terms

• Atrial Fibrillation
• Atrial Fibrillation and Flutter
• Atrial Flutter
• Atrial Flutter Typical

Intervention

Device:
• VARIPULSE™ catheter ablation
Subjects will arrive to the electrophysiology laboratory for their ablation procedure and will undergo preparation for the procedure per standard protocol. The purpose of an ablation procedure is to scar or destroy the heart tissue causing the atrial fibrillation. The current FDA approved ablation treatments commonly use freezing, radio frequency, or laser, delivered through a catheter that is threaded through blood vessels to the heart, as the energy source to destroy the abnormal tissue. The BWI IRE VARIPULSE ablation system used in this study uses a type of energy source called pulse field. Pulse field ablation applies ultra-rapid (less than 1 second) electrical fields to the heart muscle to destroy the abnormal tissue. This type of energy is thought to safer and more effective at treating atrial fibrillation. ? For a lesion set that cannot be performed using the VARIPULSE catheter technology, a conventional FDA-approved RF ablation

Locations

Country	Name	City	State
United States	Icahn School of Medicine at Mount Sinai	New York	New York

Sponsors (1)

Lead Sponsor	Collaborator
Vivek Reddy

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of participants with acute procedural success	Acute procedural success is defined according to the type of arrhythmia, for example: Entrance block in all targeted PVs for patients treated for atrial fibrillation (Both first and Re-Do); Termination of atrial flutters for patients presenting in atrial flutter.	up to 12 months post-procedure
Secondary	Percentage of time spent in atrial flutter/fibrillation/tachycardia	Percentage of time spent in atrial flutter/fibrillation/tachycardia as noted on CIED interrogation.	up to 12 months post-procedure
Secondary	Percentage of patients with no evidence of atrial fibrillation/flutter or tachycardia of more than 30 seconds of duration	The percentage of patients with no evidence of atrial fibrillation/flutter or tachycardia of more than 30 seconds of duration as noted by implantable device after the 3-month blanking period until the end of 12 months of follow-up	after 3-month blanking period until end of 12 months of follow-up
Secondary	Percentage of patients presenting with persistent atrial fibrillation with no evidence of atrial fibrillation/flutter or tachycardia of more than 30 seconds	The percentage of patients presenting with persistent atrial fibrillation with no evidence of atrial fibrillation/flutter or tachycardia of more than 30 seconds of duration as noted by implantable device after the 3-month blanking period until the end of 12 months of follow up in patients not taking anti-arrhythmic medications	after 3-month blanking period until end of 12 months of follow-up
Secondary	Percentage of patients who do not report recurrent of symptomatic arrhythmias	The percentage of patients who do not report recurrent of symptomatic arrhythmias as noted during telephone or office follow up after the 3-month blanking period until the end of 12 months of follow up	after 3-month blanking period until end of 12 months of follow-up
Secondary	Percentage of patients taking anti-arrhythmic medications with no evidence of atrial fibrillation/flutter or tachycardia of more than 30 seconds	The percentage of patients with no evidence of atrial fibrillation/flutter or tachycardia of more than 30 seconds of duration as noted by implantable device after the 3-month blanking period until the end of 12 months of follow up in patients who are taking anti-arrhythmic medications	after 3-month blanking period until end of 12 months of follow-up
Secondary	Percentage of patients not taking anti-arrhythmic medications with no evidence of atrial fibrillation/flutter or tachycardia of more than 30 seconds of duration	The percentage of patients with no evidence of atrial fibrillation/flutter or tachycardia of more than 30 seconds of duration as noted by implantable device after the 3-month blanking period until the end of 12 months of follow up in patients who not taking anti-arrhythmic medications	after 3-month blanking period until end of 12 months of follow-up
Secondary	Durability of lesion sets in any patient that undergoes a second procedure	Durability of lesion sets in any patient that undergoes a second procedure (Block across attempted lines, absence of electrograms in targeted substrate) as measured with 3-d electroanatomic map to assess bidirectional block across ablation lines.	up to 12 months post-procedure
Secondary	Number of patient emergency room (ER) visits	Number of patient emergency room (ER) visits	up to 12 months post-procedure
Secondary	Number of patient Hospitalizations	Number of patient Hospitalizations	up to 12 months post-procedure
Secondary	Number of patients requiring cardioversion	Measured by the actual occurrence of cardioversion procedures	up to 12 months post-procedure
Secondary	Number of patients who experience repeat ablation	Number of patients who experience repeat ablation	up to 12 months post-procedure