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.
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
- Type of treatment
- Medical device, Surgery or procedure
- 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.
10 sites in 1 country
Spain10 sites, 10 recruiting
- Not yet 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
- Recruiting
Hospital Universitario de Bellvitge
Barcelona, 08907
Rodolfo San Antonio, MD, PhD, 932607500 ext. 2710, rsanantonio@bellvitgehospital.cat
Rodolfo San Antonio, MD, PhD
- Not yet 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
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 group | Role | What they receive |
|---|---|---|
| Cardioneuroablation | Experimental | Bi-atrial ablation of GPs: CARDIONEUROABLATION (Group A, n = 45) Receives: Procedure: Cardioneuroablation |
| Dual-chamber pacemaker | Active comparator | Implant 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.
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)
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
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
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
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
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
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
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.
- First posted11 May 2023
- Study start22 Nov 2023
- Primary completion22 Nov 2026 (estimated)
- Study completion22 Feb 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (3)Papers the sponsor has linked to this study.
- Other trials for Reflex SyncopeStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Institut d'Investigació Biomèdica de Bellvitge
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Rodolfo San Antonio, Institut d'Investigació Biomèdica de Bellvitge
- Investigators
- Rodolfo San Antonio, MD, PhD, Study chair, Hospital Universitari de Bellvitge
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 21712276Aksu 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 35362165Piotrowski 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
Study at a glance
From the registry record, last updated by the sponsor on 25 Jan 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Recurrent Cardioinhibitory Reflex Syncope. PermANent PAcemaker Therapy or CardionEuroablation? A Multicenter RAndomized Clinical Trial
- ClinicalTrials.gov ID
- NCT05855603
- Acronym / sponsor ID
- PANACEA / ICPS044/22
- Conditions
- Reflex Syncope
- Keywords
- Cardioneuroablation, Permanent cardiac pacing, Vasovagal syncope
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 90 participants (estimated)
- Lead sponsor
- Institut d'Investigació Biomèdica de BellvitgeUniversity, hospital or other
- Study start
- 22 Nov 2023 (actual)
- Primary completion
- 22 Nov 2026 (estimated)
- Study completion
- 22 Feb 2027 (estimated)
- First posted
- 11 May 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Cardioneuroablation | Experimental | Procedure: CardioneuroablationBi-atrial ablation of GPs: CARDIONEUROABLATION (Group A, n = 45) |
| Dual-chamber pacemaker | Active comparator | Device: Permanent pacemaker therapyImplant of a dual-chamber CLS PACEMAKER* (Group B, n = 45). *or failing this, a dual-chamber pacemaker with RDR algorithm |
Who may qualify
- Ages
- 40 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (8 listed)
- 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.
Key exclusion criteria (5 listed)
- 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.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| CardioneuroablationGanglionated 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. | Procedure or surgery | Cardioneuroablation |
| Permanent pacemaker therapyAll 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). | Device | Dual-chamber pacemaker |
Primary outcome
To determine the efficacy of CNA in the treatment of cardioinhibitory reflex syncope in comparison to pacemaker therapy.
Time frame: 12 months
Differences in 12-month syncope-free survival between the 2 groups
7 secondary outcomes
To evaluate the incidence of complications in the short and long terms for CNA compared to pacemaker therapy
Time frame: 1 and 12 months
In patients undergoing CNA, evaluation of the degree of long-term reinnervation using the tilt table test (HUTT)
Time frame: 1 and 12 months
In patients undergoing CNA, evaluation of the degree of long-term reinnervation using the atropine test
Time frame: 1 and 12 months
To determine which of the 2 strategies, CNA or cardiac pacing, is superior at preventing a composite of syncope and presyncope
Time frame: 12 months
Evaluations of changes in quality of life, comparing the two therapies
Time frame: 12 months
To determine if CNA produces variations in the QTc interval
Time frame: 12 months
To determine if CNA produces variations in the burden of atrial or ventricular arrhythmias compared to pacemaker therapy
Time frame: 12 months
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 25 Jan 2024.
- Results publication: PubMed 21712276Pachon 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.
- Results publication: PubMed 35362165Aksu 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.
- Results publication: PubMed 36114133Piotrowski 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.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Rodolfo San Antonio, MD, PhD study chair
Hospital Universitari de Bellvitge
10 sites in 1 country: see every site and its status.
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.