NCT05677516

Brief Summary

Pulmonary vein isolation (PVI) is a proven, high-efficiency treatment for atrial fibrillation (AF). Performed, among others, using cryoablation, pulsed field ablation (PFA) or radiofrequency (RF) ablation. It has been shown that its effectiveness significantly increases when the PVI procedure is combined with cardioneuroablation (CNA). The autonomic nervous system - ganglionated plexi (GP), the target of the CNA, are the endings of the vagal nerve and are located in the neighborhood of the pulmonary veins ostia. Places that, in many cases, are unintentionally damaged during PVI. Varying degrees of injury to the GP during PVI indicate that the group of patients undergoing PVI is heterogeneous in this regard, and the effectiveness of PVI may vary. Vagal nerve endings damage during CNA abolishes or modifies its activity, which is manifested by the acceleration of sinus rhythm and increased atrioventricular conduction efficiency. Unintended CNA is not observed in every PVI procedure. The severity of the unintended CNA effect and its duration also vary. THE STUDY OBJECTIVES:

  1. 1.Frequency of unintentional CNA occurrence during PVI
  2. 2.Duration effect of CNA after unintentional CNA
  3. 3.Evaluation of the relationship between the different kinds of energy - cryo, pulsed field) and RFwith the unintentional CNA frequency occurrence and durability effect
  4. 4.Clinical significance evaluation of the new assessment method of the CNA effectiveness with the measure of the cSNRT and the sinus rate after its return, measured before and after PVI
  5. 5.Assessment of clinical significance for CNA evaluation of the electrophysiological parameters of AV node conduction efficiency, such as PQ interval, AH interval, HV interval, and Wenckebach's point. Parameters will be examined before and after PVI.
  6. 6.PVI efficacy evaluation with the AF and Sick Sinus Syndrome treatment, especially with the elimination of the indications for the PM implantation (sinus bradycardia, AV conduction disorders)
  7. 7.Assessment of sinus rhythm maintenance after PVI with unintentional CNA and without unintentional CNA
  8. 8.Assessment of ventricular rate control during AF burden after unintentional CNA
  9. 9.The search for new parameters evaluating the effectiveness and degree of CNA, such as the change in SR frequency after its return, may prove helpful and allow for resignation or significantly reduce the use of the complicated protocol of extracardiac vagal ganglion stimulation (ECVS) as a method to verify the effectiveness CNAs.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Dec 2021

Geographic Reach
1 country

2 active sites

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

December 23, 2021

Completed
1 year until next milestone

First Submitted

Initial submission to the registry

December 23, 2022

Completed
18 days until next milestone

First Posted

Study publicly available on registry

January 10, 2023

Completed
12 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 23, 2023

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 23, 2023

Completed
Last Updated

January 10, 2023

Status Verified

December 1, 2022

Enrollment Period

2 years

First QC Date

December 23, 2022

Last Update Submit

December 23, 2022

Conditions

Keywords

pulmonary vains isolation, catdioneuroablation, cardioneuromodultion

Outcome Measures

Primary Outcomes (3)

  • Acceleration and maintenance of a faster sinus rhythm after PVI

    Based on EPS before and after PVI and Holter ECG before and after PVI and after 3 months of follow-up.

    3 months of follow-up

  • Improvement of AV conduction efficiency and its durability after PVI

    Based on EPS before and after PVI and Holter ECG before and after PVI and after 3 months of follow-up.

    3 months of follow-up

  • Recurrence of AF during the observation period.

    Based on Holter ECG and survey after 3 months of follow-up.

    3 months of follow-up

Secondary Outcomes (1)

  • AF recurrence with the need to increase doses of heart rate control drugs.

    3 months of follow-up

Study Arms (4)

Group 1

Patients undergoing cryoablation of pulmonary veins with paroxysmal or persistent AF with ongoing AF during ablation.

Procedure: ablation- pulmonary vain isolation- crioablationProcedure: Electrophysiological study (EPS)Diagnostic Test: Holter EKGOther: Questionnaire

Group 2

Patients undergoing cryoablation of pulmonary veins with paroxysmal AF, in sinus rhythm during the procedure.

Procedure: ablation- pulmonary vain isolation- crioablationProcedure: Electrophysiological study (EPS)Diagnostic Test: Holter EKGOther: Questionnaire

Group 3

Patients undergoing pulmonary veins isolation with PFA with paroxysmal AF, in sinus rhythm during the procedure.

Procedure: ablation- pulmonary vain isolation- pulsed field ablation (PFA)Procedure: Electrophysiological study (EPS)Diagnostic Test: Holter EKGOther: Questionnaire

Group 4

Patients undergoing RF ablation of the pulmonary veins using an electroanatomical system with paroxysmal AF, in sinus rhythm during the procedure.

Procedure: ablation- pulmonary vain isolation- radiofrequency ablation (RF)Procedure: Electrophysiological study (EPS)Diagnostic Test: Holter EKGOther: Questionnaire

Interventions

Pulmonary vein isolation is the electrical isolation of the pulmonary veins from the left atrium. It can be performed using the cryoablation technique. The procedure begins with venous access through the femoral vein through which catheters and electrodes are inserted. Then, the left atrium is accessed through a transseptal puncture and the pulmonary veins are isolated using a cryoablation balloon. Cryoablation procedures are performed under local anesthesia. The procedure is performed using X-ray fluoroscopy.

Group 1Group 2

Pulmonary vein isolation is the electrical isolation of the pulmonary veins from the left atrium. It can be performed using the pulsed field ablation (PFA) technique. The procedure begins with venous access through the femoral vein through which catheters and electrodes are inserted. Then, the left atrium is accessed through a transseptal puncture and the pulmonary veins are isolated with a PFA electrode. PFA procedures are performed under general anesthesia. The procedure is performed using X-ray fluoroscopy.

Group 3

Pulmonary vein isolation is the electrical isolation of the pulmonary veins from the left atrium. It can be performed using the radiofrequency ablation (RF) technique. The procedure begins with venous access through the femoral vein through which catheters and electrodes are inserted. Then, the left atrium is accessed through a transseptal puncture and the pulmonary veins are isolated with a RF electrode. RF procedures are performed under local anesthesia. The procedure is performed using X-ray fluoroscopy.

Group 4

In the electrophysiological study (EPS), electrophysiological parameters such as the recovery time of sinus rhythm (SNRT), Wenckebach's point, AH and HV intervals are measured. The examination begins with venous access through the femoral vein. Then, diagnostic electrodes are inserted into the right atrium, right ventricle and coronary sinus, with which electrophysiological tests are performed. The SNRT is measured after 60 seconds of atrial pacing with a 600ms cycle. The Wencjabach point is determined by stimulation in the incremental protocol. AV and HV intervals are measured during sinus rhythm using an electrode placed on the bundle of His. EPS is performed under local anesthesia. EPS will be performed both before and after pulmonary vein isolation. In patients with atrial fibrillation, during ablation, only the HV interval will be measured. The procedure is performed using X-ray fluoroscopy.

Group 1Group 2Group 3Group 4
Holter EKGDIAGNOSTIC_TEST

Holter ECG is a 24-hour, non-invasive ECG recording using a portable recorder and electrodes placed on the patient's chest. The Holter ECG will be performed three times: on the day preceding and on the first day after pulmonary veins isolation, and after 3 months of observation.

Group 1Group 2Group 3Group 4

The survey will be conducted after 3 months of observation and will include questions about the number of hospitalizations due to atrial fibrillation, heart palpitations, changes in pharmacotherapy.

Group 1Group 2Group 3Group 4

Eligibility Criteria

Age18 Years - 85 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

The study group will consist of patients aged 18-85. With paroxysmal or persistent atrial fibrillation. Qualified for PVI according to the guidelines of the European Society of Cardiology.

You may qualify if:

  • Patients qualified for PVI due to paroxysmal or persistent atrial fibrillation.
  • Signed and dated written informed consent prior to admission to the trial.

You may not qualify if:

  • Any underwent cardiac ablation.
  • A history of cardiac surgery.
  • Pregnancy.
  • Diseases affecting the autonomic nervous system.
  • Change in heart rhythm during PVI, with no conversion to the primary rhythm at the end of the procedure.
  • Cardiac pacing during Holter ECG monitoring.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

4th Military Hospital, Cardiology Department

Wroclaw, Lower Silesian Voivodeship, 50-981, Poland

RECRUITING

Polish-American Heart Clinics Cardiovascular Center in Dąbrowa Górnicza, American Heart of Poland Group

Dąbrowa Górnicza, Silesian Voivodeship, 41-300, Poland

RECRUITING

Related Publications (5)

  • Hindricks G, Potpara T, Dagres N, Arbelo E, Bax JJ, Blomstrom-Lundqvist C, Boriani G, Castella M, Dan GA, Dilaveris PE, Fauchier L, Filippatos G, Kalman JM, La Meir M, Lane DA, Lebeau JP, Lettino M, Lip GYH, Pinto FJ, Thomas GN, Valgimigli M, Van Gelder IC, Van Putte BP, Watkins CL; ESC Scientific Document Group. 2020 ESC Guidelines for the diagnosis and management of atrial fibrillation developed in collaboration with the European Association for Cardio-Thoracic Surgery (EACTS): The Task Force for the diagnosis and management of atrial fibrillation of the European Society of Cardiology (ESC) Developed with the special contribution of the European Heart Rhythm Association (EHRA) of the ESC. Eur Heart J. 2021 Feb 1;42(5):373-498. doi: 10.1093/eurheartj/ehaa612. No abstract available.

    PMID: 32860505BACKGROUND
  • Katritsis DG, Pokushalov E, Romanov A, Giazitzoglou E, Siontis GC, Po SS, Camm AJ, Ioannidis JP. Autonomic denervation added to pulmonary vein isolation for paroxysmal atrial fibrillation: a randomized clinical trial. J Am Coll Cardiol. 2013 Dec 17;62(24):2318-25. doi: 10.1016/j.jacc.2013.06.053. Epub 2013 Aug 21.

    PMID: 23973694BACKGROUND
  • Aksu T, Guler TE, Bozyel S, Yalin K, Gopinathannair R. Why is pulmonary vein isolation not enough for vagal denervation in all cases? Pacing Clin Electrophysiol. 2020 May;43(5):520-523. doi: 10.1111/pace.13922. Epub 2020 May 2.

    PMID: 32324285BACKGROUND
  • Sakamoto S, Schuessler RB, Lee AM, Aziz A, Lall SC, Damiano RJ Jr. Vagal denervation and reinnervation after ablation of ganglionated plexi. J Thorac Cardiovasc Surg. 2010 Feb;139(2):444-52. doi: 10.1016/j.jtcvs.2009.04.056. Epub 2009 Sep 9.

    PMID: 19740492BACKGROUND
  • Yorgun H, Aytemir K, Canpolat U, Sahiner L, Kaya EB, Oto A. Additional benefit of cryoballoon-based atrial fibrillation ablation beyond pulmonary vein isolation: modification of ganglionated plexi. Europace. 2014 May;16(5):645-51. doi: 10.1093/europace/eut240. Epub 2013 Aug 16.

    PMID: 23954919BACKGROUND

MeSH Terms

Conditions

Atrial Fibrillation

Interventions

Electrocardiography, AmbulatorySurveys and Questionnaires

Condition Hierarchy (Ancestors)

Arrhythmias, CardiacHeart DiseasesCardiovascular DiseasesPathologic ProcessesPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

ElectrocardiographyHeart Function TestsDiagnostic Techniques, CardiovascularDiagnostic Techniques and ProceduresDiagnosisElectrodiagnosisMonitoring, AmbulatoryMonitoring, PhysiologicData CollectionEpidemiologic MethodsInvestigative TechniquesHealth Care Evaluation MechanismsQuality of Health CareHealth Care Quality, Access, and EvaluationPublic HealthEnvironment and Public Health

Central Study Contacts

Przemysław Skoczyński, PhD

CONTACT

Bruno Hrymniak, MD

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Target Duration
3 Months
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
PhD

Study Record Dates

First Submitted

December 23, 2022

First Posted

January 10, 2023

Study Start

December 23, 2021

Primary Completion

December 23, 2023

Study Completion

December 23, 2023

Last Updated

January 10, 2023

Record last verified: 2022-12

Data Sharing

IPD Sharing
Will not share

The data will be collected in a database accessible only to the named researchers.

Locations