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Reflex SyncopePANACEANCT05855603

Cardioinhibitory Reflex Syncope. Permanent Pacemaker Therapy or Cardioneuroablation?

A study testing Cardioneuroablation and Permanent pacemaker therapy in people with Reflex Syncope, run by Institut d'Investigació Biomèdica de Bellvitge at 10 sites in Spain.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

Reflex syncope is the most common form of syncope. It can lead to injuries and affect quality of life. Nonpharmacological and medical therapies have limited effectiveness. In certain patients, cardiac pacing seem to be beneficial. Read more about this study

Who is it for?
Ages 40 years and older
Conditions the study is for
Reflex Syncope
What is being tested?
Cardioneuroablation and Permanent pacemaker therapy
Could I receive a placebo?
No, everyone receives an active treatment
How many people
90 participants
Where
10 sitesSpain
Study dates
22 Nov 2023to 22 Feb 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 40 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Aged more than 40 years.
  • Having a 12-month history that includes at least two documented episodes of spontaneous reflex syncope or one episode that led to injury in addition to at least two presyncopal events, refractory to all recommended types of standard treatment.
  • Bradycardia-syncope correlation (at least 3 seconds of asystole due to sinus arrest or atrio-ventricular block) confirmed by ECG during spontaneous syncope.
  • If lacking ECG evidence during spontaneous syncope, a cardioinhibitory response (VASIS type 2A or 2B) on tilt test.
  • Displaying indicators for pacing such as those suggested in the ESC guidelines for a class I recommendation for patients with reflex syncope.
  • Significantly decreased quality of life due to syncope.
  • Sinus rhythm on ECGs.
  • Obtained written informed consent.

Who cannot join

  • Intrinsic sinus or atrioventricular nodal disease with a proven indication for permanent pacemaker implantation.
  • Evidence of structural heart disease.
  • Contraindications to ablation in the right or left atrium.
  • Life expectancy <12 months.
  • Lacking willingness to comply with the randomization procedure.

Trial locations and contacts

10 sites in 1 country. Contact the study team or a site near you to ask about taking part.

Rodolfo San Antonio, MD, PhD contact

932607500 ext. 2710

rsanantonio@bellvitgehospital.cat

10 sites in 1 country

Spain10 sites, 10 recruiting
  • Hospital del Mar

    Barcelona, 08003

    Ermengol Vallès, MD, PhD

    Ermengol Vallès, MD, PhD

    Not yet recruiting
  • Hospital de la Santa Creu i Sant Pau

    Barcelona, 08025

    José Guerra, MD, PhD

    José Guerra, MD, PhD

    Not yet recruiting
  • Hospital Universitario de Bellvitge

    Barcelona, 08907

    Rodolfo San Antonio, MD, PhD, 932607500 ext. 2710, rsanantonio@bellvitgehospital.cat

    Rodolfo San Antonio, MD, PhD

    Recruiting
  • Hospital Universitari General de Castellón

    Castellon, Castellón, 12004

    Clara Gunturiz, MD

    Clara Gunturiz, MD

    Not yet recruiting
  • Hospital Universitari Dr. Josep Trueta

    Girona, 17007

    Emilce Trucco, MD

    Emilce Trucco, MD

    Not yet recruiting
  • Hospital Universitario San Juan de Alicante

    Sant Joan d'Alacant, Alicante, 03550

    José Moreno-Arribas, MD, PhD

    José Moreno-Arribas, MD, PhD

    Not yet recruiting
  • Hospital Universitario Nuestra Señora de Candelaria

    Santa Cruz de Tenerife, 38010

    Luis Álvarez-Acosta, MD

    Luis Álvarez-Acosta, MD

    Not yet recruiting
  • Hospital Universitari i Politècnic La Fe

    Valencia, 46026

    Maite Izquierdo, MD, PhD

    Maite Izquierdo, MD, PhD

    Not yet recruiting
  • Hospital Universitario Álvaro Cunqueiro de Vigo

    Vigo, Pontevedra, 36312

    Enrique García-Campo, MD

    Enrique García-Campo, MD

    Not yet recruiting
  • Hospital Clínico Universitario Lozano Blesa

    Zaragoza, 50009

    Javier Ramos-Maqueda, MD, PhD

    Javier Ramos-Maqueda, MD, PhD

    Not yet recruiting

Other trials in Spain

About this study

Official title: Recurrent Cardioinhibitory Reflex Syncope. PermANent PAcemaker Therapy or CardionEuroablation? A Multicenter RAndomized Clinical Trial

Reflex syncope is the most common form of syncope. It can lead to injuries and affect quality of life. Nonpharmacological and medical therapies have limited effectiveness. In certain patients, cardiac pacing seem to be beneficial. More recently cardioneuroablation (CNA) has emerged as a novel therapy for reflex syncope. The investigators aim to determine whether CNA is more effective than cardiac pacing at reducing the rate of cardioinhibitory-type reflex syncope.

Read the detailed description

Reflex or neurally mediated syncope is the most common form of syncope in any setting and at all ages. It is associated with an autonomic imbalance in which vagal hyperactivity predominates, resulting in vasodilation or bradycardia or both, thereby producing a fall in global cerebral perfusion. It is divided into three types: vasovagal, situational, and carotid sinus syndrome.

Reflex syncope is benign and usually occurs in healthy people; however, very frequent syncope or events without prodromal symptoms can lead to injuries and affect long-term quality of life. Nonpharmacological and medical therapies proven effective in randomized clinical trials are scarce. In certain patients with frequent and burdensome cardioinhibitory reflex syncope, dual-chamber cardiac pacemakers seem to be beneficial. More recently, catheter-based cardiac autonomic modulation, or cardioneuroablation (CNA), has emerged as a novel therapy for reflex syncope, and positive results in small open-label cohort studies, and more recently in the first randomized study, have been reported.

The literature provides sufficient evidence that cardiac pacing should be considered in select patients affected by severe forms of reflex syncope with frequent recurrence and a high risk of injury. Current guidelines suggest that pacemaker therapy should be considered in patients aged more than 40 years with frequent recurrent reflex syncope when asystole has been documented, induced by either carotid sinus massage (CSM) or the head-up tilt test (HUTT), or recorded using an electrocardiogram (ECG) monitoring system (≥3 seconds if syncope, ≥6 seconds if asymptomatic).

Cardiac autonomic system modulation by endocardial ablation targeting atrial ganglionated plexi (GPs), or CNA, has been recently proposed as a novel therapy for reflex syncope.

Cardioneuroablation was introduced by Pachon et al. in 2005. In their initial study, twenty-one symptomatic patients with vasovagal syncope (6 patients), functional high-degree atrio-ventricular block (7 patients), and/or functional sinus node dysfunction (13 patients), were treated with CNA without complications. Follow-up for a mean of 9.2 months demonstrated symptom relief for all patients. After this initial description, several small studies and case series confirmed the efficacy of this approach. In a recent randomized prospective study, Piotrowski et al. documented that not only could CNA significantly reduce recurrences of syncopal episodes in patients with vasovagal syncope, it could also improve quality of life.

The primary strength of this therapeutic approach is that it avoids pacemaker implant, a procedure with a significant complication rate during long-term follow-up in a population composed predominantly of young and otherwise healthy patients.

The excellent results reproduced by many investigators worldwide suggest that CNA should be considered in patients with reflex syncope, especially those who display an important cardioinhibitory component of syncope. However, given that current evidence is limited, and the procedure carries potential risk, a randomized clinical trial to assess the true benefit of CNA and to compare this technique with pacemaker implantation should be performed. Results could guide the physician to the best current choice in this scenario.

Conditions
Reflex Syncope
Being tested
Cardioneuroablation, Permanent pacemaker therapy
Keywords
Cardioneuroablation, Permanent cardiac pacing, Vasovagal syncope
Medical subject headings
Syncope, Vasovagal

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • CardioneuroablationProcedure or surgery

    Ganglionated plexi will be localized using an empirical anatomical approach and/or a fractionated electrogram-based strategy.

    Point-by-point ablation will be performed using radiofrequency energy and an irrigated tip contact force sensing ablation catheter in a power control mode (35-50 W; AI, 350-500; LSI, 4.5-5.5). The right superior GP (RSGP), left superior GP (LSGP) and posterior left GP (PMLGP) will be targeted during CNA. Radiofrequency applications in other GPs will be left at the discretion of the operator.

    At the end of the procedure, another EP study and atropine test will be performed. Clinical endpoints for completion of the CNA will be: 1) a HR increase >20% if the CNA was performed under general anesthesia/deep sedation; 2) improved electrophysiological parameters; 3) significant reduction in atropine response (HR increase <10% after atropine); and 4) in case of using extracardiac vagal stimulation, lack of response.

  • Permanent pacemaker therapyDevice

    All patients in the pacemaker group will receive a dual-chamber pacemaker that has the ability to be programmed in the DDD-CLS algorithm mode (or failing this, a dual-chamber pacemaker with RDR algorithm).

Study groups in NCT05855603
Study groupRoleWhat they receive
CardioneuroablationExperimentalBi-atrial ablation of GPs: CARDIONEUROABLATION (Group A, n = 45)
Receives: Procedure: Cardioneuroablation
Dual-chamber pacemakerActive comparatorImplant of a dual-chamber CLS PACEMAKER* (Group B, n = 45). *or failing this, a dual-chamber pacemaker with RDR algorithm
Receives: Device: Permanent pacemaker therapy

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. To determine the efficacy of CNA in the treatment of cardioinhibitory reflex syncope in comparison to pacemaker therapy.

    Differences in 12-month syncope-free survival between the 2 groups

    Measured: 12 months

Secondary outcomes (7)
  1. To evaluate the incidence of complications in the short and long terms for CNA compared to pacemaker therapy

    Pacemaker and CNA complication rates at 1 and 12 months

    Measured: 1 and 12 months

  2. In patients undergoing CNA, evaluation of the degree of long-term reinnervation using the tilt table test (HUTT)

    Changes in response to HUTT (type 1-3) at baseline, 1 and 12 months

    Measured: 1 and 12 months

  3. In patients undergoing CNA, evaluation of the degree of long-term reinnervation using the atropine test

    Changes in response (maximum heart rate) to atropine test at baseline, 1 and 12 months

    Measured: 1 and 12 months

  4. To determine which of the 2 strategies, CNA or cardiac pacing, is superior at preventing a composite of syncope and presyncope

    Differences in 12-month syncope- and presyncope-free survival between the 2 groups

    Measured: 12 months

  5. Evaluations of changes in quality of life, comparing the two therapies

    Using the Impact of Syncope on Quality-of-life questionnaire (University of Calgary). It consists of 9 questions with 6 choices and 3 questions with 5 choices. The overall maximum score is 57. The higher the score, the poorer the QOL is

    Measured: 12 months

  6. To determine if CNA produces variations in the QTc interval

    The QTc interval will be measured at minimum, average and maximum heart rate using a 24-hour holter monitoring

    Measured: 12 months

  7. To determine if CNA produces variations in the burden of atrial or ventricular arrhythmias compared to pacemaker therapy

    Arrhythmias will be detected by implantable loop recorder in the group A (CNA) vs. by the pacemaker itself in group B

    Measured: 12 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted11 May 2023
  2. Study start22 Nov 2023
  3. Primary completion22 Nov 2026 (estimated)
  4. Study completion22 Feb 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
90 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05855603
Sponsor's protocol ID
ICPS044/22
Acronym
PANACEA
Status last verified
Jan 2024
First submitted
20 Apr 2023
Last updated
25 Jan 2024
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Pachon JC, Pachon EI, Cunha Pachon MZ, Lobo TJ, Pachon JC, Santillana TG. Catheter ablation of severe neurally meditated reflex (neurocardiogenic or vasovagal) syncope: cardioneuroablation long-term results. Europace. 2011 Sep;13(9):1231-42. doi: 10.1093/europace/eur163. Epub 2011 Jun 28.

    PubMed 21712276
  • Aksu T, Gupta D, D'Avila A, Morillo CA. Cardioneuroablation for vasovagal syncope and atrioventricular block: A step-by-step guide. J Cardiovasc Electrophysiol. 2022 Oct;33(10):2205-2212. doi: 10.1111/jce.15480. Epub 2022 Apr 9.

    PubMed 35362165
  • Piotrowski R, Baran J, Sikorska A, Krynski T, Kulakowski P. Cardioneuroablation for Reflex Syncope: Efficacy and Effects on Autonomic Cardiac Regulation-A Prospective Randomized Trial. JACC Clin Electrophysiol. 2023 Jan;9(1):85-95. doi: 10.1016/j.jacep.2022.08.011. Epub 2022 Aug 28.

    PubMed 36114133

Questions about this trial

What is this clinical trial studying?

A study testing Cardioneuroablation and Permanent pacemaker therapy in people with Reflex Syncope, run by Institut d'Investigació Biomèdica de Bellvitge at 10 sites in Spain.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 8 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 25 Jan 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 10 sites in Spain. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Rodolfo San Antonio, MD, PhD (932607500 ext. 2710, rsanantonio@bellvitgehospital.cat), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

To determine the efficacy of CNA in the treatment of cardioinhibitory reflex syncope in comparison to pacemaker therapy. (time frame: 12 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT05855603, which also lists 3 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 25 Jan 2024.

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