Brugada Syndrome Clinical Trial
— UNCOVERBrSOfficial title:
Brugada Syndrome Substrate Characterization and Ablation: Insights From ECG BrS Type I Pattern, Novel Prognostic Index dST-Tiso and High Density Mapping
Independent, single center, prospective study, to evaluate the efficacy, in consecutive BrS patients undergoing catheter ablation, at medium-long term follow-up after epicardial substrate homogenization. The target area is defined collecting signals using high density and high resolution mapping with equi-spaced electrode array. The ablation of abnormal fragmented prolonged low-frequency ventricular electrograms is performed by contact force catheter.
Status | Recruiting |
Enrollment | 20 |
Est. completion date | June 30, 2025 |
Est. primary completion date | May 30, 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: 1. Symptomatic patients diagnosed with BrS-ECG pattern of types 1 and 2, both spontaneous and arising after Ajmaline tests, already implanted with an ICD. Symptomatic patients are defined as those who present =1 documented episode of VT / VF in the 12 months prior to enrollment. 2. Patients eligible for ablation with 3D high-density mapping system in accordance with national guidelines, IFU and according to medical decision; 3. Adult patients able to provide written informed consent Exclusion Criteria: 1. Patients unable to provide written informed consent; 2. Patients unable to guarantee their presence at future FU visits; 3. Patients who, according to medical judgment, have a life expectancy of less than 12 months; 4. Patients who have undergone cardiac ablation in the 90 days prior to enrollment. 5. Patients who have had adverse events that have not been resolved after any invasive procedure; 6. Women potentially pregnant or planning to become pregnant. |
Country | Name | City | State |
---|---|---|---|
Italy | Maria Cecilia Hospital | Cotignola | Ravenna |
Lead Sponsor | Collaborator |
---|---|
Maria Cecilia Hospital |
Italy,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Percentage of patients free from any clinical ventricular arrhythmia at a 3, 6-months and 12-months follow-up from the procedure. | The primary aim of the study is the rate of success at medium-long term follow-up after epicardial substrate homogenization (ablating abnormal fragmented prolonged low-frequency ventricular electrograms) in consecutive brugada patients undergoing catheter ablation.
The medium-long term success of the ablation is defined in terms of percentage of patients free from any clinical ventricular arrhythmia at a 3, 6-months and 12-months follow-up from the procedure. |
12-months | |
Secondary | Collecting and analyzing data concerning late potential and voltage maps using different settings, vector data and speed maps, could be useful to better understand and describe the mechanism of this pathology. | • Comparison among different setting of voltage map (OT vs Standard acquisition) | 12 months |
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT05048602 -
Drug-induced Brugada Syndrome Research Database
|
||
Terminated |
NCT00701077 -
DAPERB 3,4-DiAminoPyridine and Electrophysiological Response in Brugada Syndrome
|
Phase 3 | |
Recruiting |
NCT03435393 -
Ripple Mapping for Epicardial Mapping of Brugada Syndrome
|
N/A | |
Active, not recruiting |
NCT02933437 -
The Response To Ajmaline Provocation in Healthy Subjects
|
Phase 2 | |
Active, not recruiting |
NCT04257994 -
Distribution of Cell-cell Junction Proteins in Arrhythmic Disorders
|
||
Recruiting |
NCT05685134 -
Invasive and Clinical Features in Patients With Brugada Syndrome Undergoing Catheter Ablation
|
N/A | |
Recruiting |
NCT04580992 -
Defining the Electrocardiographic Effect of Propofol on the Ajmaline Provocation Drug Challenge: A Prospective Trial
|
||
Completed |
NCT02641431 -
Epicardial Ablation in Brugada Syndrome
|
N/A | |
Completed |
NCT03182777 -
Safety of Local Dental Anesthesia in Patients With Cardiac Channelopathies
|
N/A | |
Completed |
NCT00292032 -
Registry of Unexplained Cardiac Arrest
|
||
Completed |
NCT04124237 -
Long Term Monitoring for Risk of Sudden Death
|
||
Completed |
NCT02344277 -
Evaluation of Subcutaneous Implantable Cardiac Defibrillator in Brugada Patients
|
||
Completed |
NCT04650009 -
Physical Activity in Children With Inherited Cardiac Diseases
|
||
Recruiting |
NCT04808193 -
European Perioperative Brugada Survey
|
N/A | |
Recruiting |
NCT03491475 -
Echocardiography During Ajmaline Test
|
||
Recruiting |
NCT05521451 -
Clinical Cohort Study - TRUST
|
||
Recruiting |
NCT03485508 -
The Brugada Syndrome: a Follow-up Study
|
||
Completed |
NCT00702117 -
Ajmaline Utilization in the Diagnosis and Treatment of Cardiac Arrhythmias
|
Phase 4 | |
Recruiting |
NCT02704416 -
Ablation in Brugada Syndrome for the Prevention of VF
|
N/A | |
Recruiting |
NCT03775954 -
Fetal Electrophysiologic Abnormalities in High-Risk Pregnancies Associated With Fetal Demise
|