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NCT Number: NCT06288633

Cardioneuroablation for Bradyarrhythmia

This is a multicenter prospective randomized blind controlled trial with a sham procedure group of the efficacy and safety of cardioneuroablation as a method of treating symptomatic bradycardia without a permanent pacemaker implantation

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Almazov National Medical Research Centre

Saint Petersburg, Russia

Location status: Recruiting

Location contact

Shlyakhto

CONTACT

+78127023749

About this study

Catheter ablation is a common treatment for cardiac arrhythmias. Some patients with AF ablation or AVNRT experience acceleration of sinus rhythm, the most likely cause of which is modification of autonomic tone caused by inadvertent damage to intramural autonomic ganglia and fibers. Intentional damage to these plexuses has become known as cardioneuroablation (CNA) and is currently used in patients with tachycardia-bradycardia syndrome, vegetatively caused sinus node dysfunction and atrioventricular conduction disorders, vasovagal syncopal conditions developing in a cardioinhibitory type.

It is suggested that in some patients CNA may become an alternative to permanent pacemaker for the treatment of symptomatic bradyarrhythmias.

This is a multicentre randomised clinical study evaluating the efficacy of cardioneuroablation for severe bradycardia due to sinus node dysfunction and/or atrioventricular nide dysfunction versus a sham procedure.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Any of the following variants of bradyarrhythmia in patients aged 18-65 years:

(1.1.) Symptomatic sinus bradycardia or bradycardia due to atrioventricular blockade, including transient.

(1.2.) Severe asymptomatic sinus bradycardia with a rhythm frequency of <30 beats/min.

(1.3.) Transient atrioventricular block of II-III degree or permanent block of II degree.

(1.4.) Repeated fainting or pre-fainting states with a proven association with bradycardia (without injury).

(1.5.) Rhythm pauses >6 seconds.

In combination with the following two criteria:

  • Positive reaction to physical activity and/or atropine test:

(2.1.) Increase in sinus rhythm frequency ≥25% or >90 beats/min. (2.2.) The transition of atrioventricular blockade of the II-III degree to the 1st degree or complete normalization of atrioventricular conduction at the sinus rhythm.

  • Sinus rhythm at the time of switching on

Exclusion criteria

  • Anamnesis of injury during syncopation due to bradycardia, except in the case when the patient refused to implant an electrocardiostimulator for his own reasons in writing;
  • Constant intake of antiarrhythmic drugs (for PVC, AF, etc.);
  • The presence of an implanted pacemaker, a heart contractility modulation device, a cardioverter defibrillator;
  • Drug-induced sinus bradycardia and/or atrioventricular block;
  • Bradycardia due to electrolyte imbalance (e.g. hyperkalemia);
  • Bradycardia due to hypothyroidism or other reversible conditions;
  • No reaction to the administration of atropine (up to a maximum dose of 0.2 mg / kg);
  • Proven association of bradyarrhythmia with episodes of apnea/hypopnea in obstructive sleep apnea syndrome;
  • Clinically significant coronary artery disease;
  • Postinfarction cardiosclerosis;
  • Hemodynamically significant congenital heart defects, including operated ones;
  • Stroke or transient ischemic attack <3 months;
  • Open heart surgery in the anamnesis;
  • Catheter interventions on coronary arteries or for cardiac arrhythmias <3 days;
  • Conditions after percutaneous coronary angioplasty <3 months;
  • Anamnesis of stable ventricular tachycardia on the background of bradycardia;
  • Pregnancy or breastfeeding period

Treatment and study plan

Ganglionated plexi ablation

Procedure

Through access in the femoral vein, a mapping or ablation-mapping catheter is inserted into the right atrium, and a three-dimensional reconstruction of the right atrium is performed using an electroanatomic mapping system. The inferior and superior vena cava, the coronary sinus are indicated.

Then a transeptal puncture is performed using a transeptal introducer and a needle for transeptal puncture under fluoroscopic control. A three-dimensional reconstruction of the left atrium is performed using an electroanatomic mapping system.

During or immediately after the creation of three-dimensional maps of both atria, areas of the typical concentration of ganglion plexuses (GP) are ablated using radiofrequency applications (30-50 Watts, 10-40 s each point). Ablated points are annotated on the three-dimensional map. GPs ablation zones are about 0.5 x 1.0 cm in size.

Electrophysiological study

Diagnostic Test

Through access in the femoral vein, a diagnostic catheter is inserted in the area of the coronary sinus under fluoroscopic control. The effective refractory period (ERP) of the atria will be measured according to the method adopted in clinical practice, namely: using a ten-pole diagnostic electrode installed in the coronary sinus, a series of eight electrical pulses with the same amplitude and frequency is applied to the atrial myocardium. Then the ninth pulse is applied with a gradual decrease in the time interval until the absence of an atrial myocardium response to the pulse is registered. The cycle of an additional, ninth pulse, in which the atrial myocardium did not respond to an electrical impulse, is considered an atrial ERP.

Primary outcomes

  1. Implantation of a permanent cardiac pacemaker

    Time frame: 12 months post procedure

    Once there is a recurrence of documented symptomatic bradycardia, a permanent pacemaker implantation is considered

Secondary outcomes

  1. Complications of cardioneuroablation

    Time frame: 30 days post procedure

    Cardiac tamponade, pericardial effusion >10 mm, esophageal damage, stroke or transient ischemic event, severe groin hematoma (hemoglobin level drop >20%), atriovenous fistula in the groin

  2. Presence of symptomatic or asymptomatic rhythm pauses >6 seconds

    Time frame: 12 months post procedure

    As detected by ECG monitoring

  3. The presence of symptomatic or asymptomatic sinus bradycardia with an average heart rate <40 beats/min in the daytime

    Time frame: 12 months post procedure

    As detected by ECG monitoring

  4. Transient or permanent atrioventricular block

    Time frame: 12 months post procedure

    As detected by ECG monitoring

  5. Orthostatic hypotension and/or bradycardia during passive orthostasis test

    Time frame: 12 months post procedure

    Tilt-testing

  6. Sinus tachycardia after cardioneuroablation

    Time frame: 30 days post procedure

    As detected by ECG monitoring, defined as daytime mean heart rate >100 bpm

  7. Implantation of a pacemaker by 24 months after randomization

    Time frame: 24 months post procedure

    Once there is a recurrence of documented symptomatic bradycardia, a permanent pacemaker implantation is considered

Study contacts

Contact information is provided by the study sponsor or research team.

Aleksandr Vakhrushev, PhD

CONTACT

[email protected]

+78127023749

Evgeny Mikhaylov, PhD, Prof.

CONTACT

[email protected]

+78127023749

Sponsors and collaborators

Lead sponsor

Federal State Budgetary Institution, V. A. Almazov Federal North-West Medical Research Centre, of the Ministry of Health

Other

Collaborators

  • City Clinical Hospital No.52 of Moscow Healthcare Department
  • Clinical City Hospital named after I.V. Davydovsky of Moscow Department of Healthcare
  • Medical Centre Hospital of the President's Affairs Administration, Republic of Kazakhstan
  • Meshalkin National Medical Research Center, Ministry of Health of Russian Federation
  • National Medical Research Center for Cardiology, Ministry of Health of Russian Federation
  • National Medical Research Center for Therapy and Preventive Medicine
  • The Federal Centre of Cardiovascular Surgery, Russia
  • Tomsk National Research Medical Center of the Russian Academy of Sciences
  • Vishnevsky Center of Surgery

Registry information

Official study title

Cardioneuroablation for Bradyarrhythmia (Sinus Node and Atrioventricular Node Dysfunction): a Sham-controlled Randomised Multicentre Trial

Acronym: CARDIOBOOST

Important dates

Study start
2024
Primary completion
2026
Study completion
2027
First posted
Mar 1, 2024
Registry last updated
Mar 5, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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