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Cardiac Autonomic Denervation for Cardio-inhibitory Syncope (CardioSync)

Primary Purpose

Bradycardia; Syncope, Syncope, Vasovagal

Status
Not yet recruiting
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
Electrophysiological study
Electrophysiological study and Right side Ganglionated Plexi ablation
Electrophysiological study and bi-atrial Ganglionated Plexi ablation
Sponsored by
University of Sao Paulo General Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Bradycardia; Syncope focused on measuring Cardiac denervation, Cardio-inhibitory syncope

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Aged between 18 and 70 years old.
  • Cardio-inhibitory response (VASIS 2A or 2B) during tilt test, or after carotid sinus massage.
  • Patients with bradycardia mediated by vagal hypertonia documented on 24-hour Holter monitoring and a clear relationship with symptoms.

Exclusion Criteria:

  • Ages under 18 and over 70
  • Presence of structural heart disease documented by echocardiography.
  • Hypothyroidism and hyperthyroidism, drug effects, obstructive sleep apnea and other causes of secondary bradycardia.
  • Anatomical disease of the conduction system.

Sites / Locations

  • University of Sao Paulo General Hospital
  • Arrhythmia and electrophysiology of the Heart Institute - University of São Paulo

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Sham Comparator

Active Comparator

Active Comparator

Arm Label

Group A

Group B

Group C

Arm Description

A diagnostic electrophysiological study will be performed in patients of group A

A electrophysiological study with cardiac denervation, with right Ganglionated Plexi ablation exclusively will be performed in patients of group B

A electrophysiological study with cardiac denervation, with right and left Ganglionated Plexi ablation will be performed in patients of group C.

Outcomes

Primary Outcome Measures

recurrence of syncope
To compare the recurrence of syncope or pre-syncope and a negative tilt test with the different techniques of electrophysiological procedures currently used.

Secondary Outcome Measures

electrocardiographic and electrophysiological parameters
Compare the following electrocardiographic and electrophysiological parameters of vagal attenuation: Heart rate (bpm - beats per minute); Internal AH (represents AV internodal conduction time, with normal values between 50-120 ms); Wenckebach cycle; Presence of Holter pauses 30 days after the intervention.

Full Information

First Posted
May 20, 2022
Last Updated
August 15, 2023
Sponsor
University of Sao Paulo General Hospital
Collaborators
Abbott
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1. Study Identification

Unique Protocol Identification Number
NCT05572034
Brief Title
Cardiac Autonomic Denervation for Cardio-inhibitory Syncope
Acronym
CardioSync
Official Title
Cardiac Autonomic Denervation for Cardio-inhibitory Syncope
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
September 1, 2023 (Anticipated)
Primary Completion Date
December 30, 2023 (Anticipated)
Study Completion Date
March 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Sao Paulo General Hospital
Collaborators
Abbott

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Background: Autonomic system modification is an established therapeutic approach that has been increasingly used for the treatment of vagal-related symptomatic bradycardia, such as cardio-inhibitory vasovagal syncope1-12. Although convincing results had been reported from small populations, a large randomized study providing robust evidence on the efficacy of this approach has not yet been performed. Hypothesis: Cardiac autonomic system modification is effective for the treatment of vagal-related symptomatic bradycardia, and is associated better clinical results as compared to placebo.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bradycardia; Syncope, Syncope, Vasovagal
Keywords
Cardiac denervation, Cardio-inhibitory syncope

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
randomized, prospective, sham controll, on a 1:1:1 basis to group A (Sham - 15 patients); group B (right sided denervation - 15 patients); and group C (bilateral denervation - 15 patients)
Masking
Participant
Masking Description
all patients will go for intervention, however they will not know which group they were randomized to
Allocation
Randomized
Enrollment
45 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Group A
Arm Type
Sham Comparator
Arm Description
A diagnostic electrophysiological study will be performed in patients of group A
Arm Title
Group B
Arm Type
Active Comparator
Arm Description
A electrophysiological study with cardiac denervation, with right Ganglionated Plexi ablation exclusively will be performed in patients of group B
Arm Title
Group C
Arm Type
Active Comparator
Arm Description
A electrophysiological study with cardiac denervation, with right and left Ganglionated Plexi ablation will be performed in patients of group C.
Intervention Type
Procedure
Intervention Name(s)
Electrophysiological study
Intervention Description
Electrophysiological study: patients in a fasting state and under total intravenous anesthesia Intracardiacelectrogramsare displayed simultaneously on a multichannel recorder. Programmed atrial and ventricular stimulation are performed to rule out sustained arrhythmias, primary conduction system dysfunction, and sick sinus syndrome.
Intervention Type
Procedure
Intervention Name(s)
Electrophysiological study and Right side Ganglionated Plexi ablation
Intervention Description
Electrophysiological study: patients in a fasting state and under total intravenous anesthesia Intracardiacelectrogramsare displayed simultaneously on a multichannel recorder. Programmed atrial and ventricular stimulation are performed to rule out sustained arrhythmias, primary conduction system dysfunction, and sick sinus syndrome. GP Mapping and Cardiac denervation: Specific atrium sites are empirically identified as GP by presumed anatomic location based on previous works (anatomic mapping): In the RA: the posterior aspect of the interatrial septum, between the posterior wall and coronary sinus ostium; and, the septal aspect of the superior vena cava junction (opposite to the LA GP tags). A 3.5-mm irrigated tip catheter will be used to deliver radiofrequency energy (50°C, 20-30 W, for 30-60 seconds) with a 17 mL/min irrigation flow.
Intervention Type
Procedure
Intervention Name(s)
Electrophysiological study and bi-atrial Ganglionated Plexi ablation
Intervention Description
Electrophysiological study: patients in a fasting state and under total intravenous anesthesia Intracardiacelectrogramsare displayed simultaneously on a multichannel recorder. Programmed atrial and ventricular stimulation are performed to rule out sustained arrhythmias, primary conduction system dysfunction, and sick sinus syndrome. GP Mapping and Cardiac denervation: Specific atrium sites are empirically identified as GP by presumed anatomic location based on previous works(anatomic mapping): In the LA: the inferior right GP (septal aspect of the right pulmonary veins [PV]) antra, and LA posterior wall. In the RA: the posterior aspect of the interatrial septum, between the posterior wall and coronary sinus ostium; and the septal aspect of the superior vena cava junction (opposite to the LA GP tags). A 3.5-mm irrigated tip catheter will be used to deliver radiofrequency energy (50°C, 20-30 W, for 30-60 seconds) with a 17 mL/min irrigation flow.
Primary Outcome Measure Information:
Title
recurrence of syncope
Description
To compare the recurrence of syncope or pre-syncope and a negative tilt test with the different techniques of electrophysiological procedures currently used.
Time Frame
24 months
Secondary Outcome Measure Information:
Title
electrocardiographic and electrophysiological parameters
Description
Compare the following electrocardiographic and electrophysiological parameters of vagal attenuation: Heart rate (bpm - beats per minute); Internal AH (represents AV internodal conduction time, with normal values between 50-120 ms); Wenckebach cycle; Presence of Holter pauses 30 days after the intervention.
Time Frame
24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Aged between 18 and 70 years old. Cardio-inhibitory response (VASIS 2A or 2B) during tilt test, or after carotid sinus massage. Patients with bradycardia mediated by vagal hypertonia documented on 24-hour Holter monitoring and a clear relationship with symptoms. Exclusion Criteria: Ages under 18 and over 70 Presence of structural heart disease documented by echocardiography. Hypothyroidism and hyperthyroidism, drug effects, obstructive sleep apnea and other causes of secondary bradycardia. Anatomical disease of the conduction system.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Mauricio I scanavacca, MD, PhD
Phone
+ 55 11 26615341
Email
mauricio.scanavacca@incor.usp.br
First Name & Middle Initial & Last Name or Official Title & Degree
Esteban W Rivarola, MD, PhD
Phone
+55 11 26615341
Email
eteban@hotmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mauricio I Scanavacca, MD, PhD
Organizational Affiliation
University of Sao Paulo - General Hospítal
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Sao Paulo General Hospital
City
Sao Paulo
State/Province
SP
ZIP/Postal Code
01246-000
Country
Brazil
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mauricio I Scanavacca, MD, PhD
Phone
+551126615341
Email
mauricio.scanavacca@gmail.com
First Name & Middle Initial & Last Name & Degree
Esteban W Rivarola, MD, PhD
Phone
+551126615341
Email
eteban@hotmail.com
First Name & Middle Initial & Last Name & Degree
Mauricio I Scanavacca, MD, PhD
First Name & Middle Initial & Last Name & Degree
Esteban W Rivarola, MD, PhD
First Name & Middle Initial & Last Name & Degree
Gabrielle D Pessente, BsC, MS
Facility Name
Arrhythmia and electrophysiology of the Heart Institute - University of São Paulo
City
São Paulo
ZIP/Postal Code
05403-900
Country
Brazil
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gabrielle D Pessente, BSc, MS
Phone
+55 11 26615712
Email
gabrielle.pessente@hc.fm.usp.br
First Name & Middle Initial & Last Name & Degree
Esteban W Rivarola, MD, PhD
First Name & Middle Initial & Last Name & Degree
Mauricio I Scanavacca, MD, PhD

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
33024505
Citation
Hardy C, Rivarola E, Scanavacca M. Role of Ganglionated Plexus Ablation in Atrial Fibrillation on the Basis of Supporting Evidence. J Atr Fibrillation. 2020 Jun 30;13(1):2405. doi: 10.4022/jafib.2405. eCollection 2020 Jun-Jul.
Results Reference
background
PubMed Identifier
34026520
Citation
Sarabanda AV, Melo SL, Rivarola E, Hachul D, Scanavacca M. Anatomically guided atrial ganglionated plexus ablation evaluated by extracardiac vagal stimulation for vagally mediated atrioventricular block. HeartRhythm Case Rep. 2021 Feb 10;7(5):301-305. doi: 10.1016/j.hrcr.2021.02.002. eCollection 2021 May. No abstract available.
Results Reference
background

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Cardiac Autonomic Denervation for Cardio-inhibitory Syncope

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