SINGLE SHOT CHAMPION

Phase 4Active Not RecruitingNCT05534581

Insel Gruppe AG, University Hospital Bern210 enrolled

Overview

Pulmonary vein isolation (PVI) is an effective treatment for atrial fibrillation (AF). Currently, Medtronic Arctic Front Cryoballoon is the most frequently used single shot technology and hence is the benchmark for upcoming technologies. A novel method, pulse-field ablation (PFA) using the FARAPULSE catheter, has recently been introduced (FARAPULSE PFA, Boston Scientific). However, whether FARAPULSE PFA provides effectiveness similar to the standard-of-practice Medtronic Arctic Front Cryoballoon is yet to be investigated. Given that FARAPULSE PFA has shown in studies not to cause any of the severe complications reported in association with traditional PVI while being highly effective, it might be even safer and more effective for use in AF ablation procedures. The aim of this trial is to compare the efficacy and safety of PVI using FARAPULSE PFA (Boston Scientific) and the Arctic Front Cryoballoon (Medtronic) in patients with symptomatic paroxysmal AF undergoing their first PVI. This is an investigator-initiated, multicenter, randomized controlled, open-label trial with blinded endpoint adjudication. Given that the Medtronic Arctic Front Cryoballoon is the standard-of-practice for PVI and the FARAPULSE PFA is the novel technology, this trial has a non-inferiority design. The null hypothesis with regards to the primary efficacy endpoint is that the FARAPULSE PFA (Boston Scientific) shows lower efficacy compared to the Arctic Front Cryoballoon (Medtronic) and that therefore more episodes of first recurrence of any atrial arrhythmia between days 91 and 365 will be observed in patients with symptomatic paroxysmal AF undergoing their first PVI. Hence, the alternative hypothesis postulates that the FARAPULSE PFA is non-inferior to the Arctic Front Cryoballoon. Rejection of the null hypothesis is needed to conclude non-inferiority.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

Interventions

PVI using the Arctic Front Cryoballoon (Medtronic)DEVICE

Patients randomized to the Arctic Front cryoballoon group will undergo PVI using the Arctic Front Cryoballoon (Medtronic). At the end of the procedure, an implantable cardiac monitor will be implanted for the purpose of continuous arrhythmia monitoring.

PVI using FARAPULSE Pulsed Field Ablation (Boston Scientific)DEVICE

Patients randomized to the Pulsed Field Ablation group will undergo PVI using the FARAPULSE PFA system (Boston Scientific). At the end of the procedure, an implantable cardiac monitor will be implanted for the purpose of continuous arrhythmia monitoring.

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Paroxysmal atrial fibrillation documented on a 12 lead ECG or Holter monitor (lasting ≥30 seconds) within the last 24 months. According to current guidelines, paroxysmal is defined as any AF that converts to sinus rhythm within 7 days either spontaneously or by pharmacological or electrical cardioversion * Candidate for ablation based on current AF guidelines * Continuous anticoagulation with Vitamin-K-Antagonists or a novel oral anticoagulant for ≥4 weeks prior to the ablation; or a transesophageal echocardiography and/or computer tomography that excludes left atrial (LA) thrombus ≤48 hours before ablation * Age of 18 years or older on the date of consent * Informed Consent as documented by signature Exclusion Criteria: * Previous left atrial (LA) ablation or LA surgery * AF due to reversible causes (e.g. hyperthyroidism, cardiothoracic surgery) * Intracardiac thrombus * Pre-existing pulmonary vein stenosis or PV stent * Pre-existing hemidiaphragmatic paralysis * Contraindication to anticoagulation or radiocontrast materials * Prior mitral valve surgery * Severe mitral regurgitation or moderate/severe mitral stenosis * Myocardial infarction during the 3-month period preceding the consent date * Ongoing triple therapy * Cardiac surgery during the three-month interval preceding the consent date or scheduled cardiac surgery/TAVI procedure * Significant congenital heart defect (including atrial septal defects or PV abnormalities but not including PFO) * NYHA class III or IV congestive heart failure * Left ventricular ejection fraction (LVEF) \<35% * Hypertrophic cardiomyopathy (wall thickness \>1.5 cm) * Significant chronic kidney disease (CKD; eGFR \<30 ml/min) * Uncontrolled hyperthyroidism * Cerebral ischemic event (stroke or TIA) during the six-month interval preceding the consent date * Ongoing systemic infections * History of cryoglobulinemia * Cardiac amyloidosis * Pregnancy * Life expectancy less than one (1) year per physician opinion * Currently participating in any other clinical trial, which may confound the results of this trial. * Unwilling or unable to comply fully with study procedures and follow-up.

Outcomes

Primary Outcomes

Time to first recurrence of any atrial tachyarrhythmia

Time to first recurrence of any atrial tachyarrhythmia (atrial fibrillation \[AF\], atrial flutter \[AFL\] or atrial tachycardia \[AT\]) between days 91 and 365 post ablation as detected on continuous implantable cardiac monitor (ICM). AF, AFL or AT will qualify as a recurrence after ablation if it lasts 120 s or longer on ICM (the minimum programmable episode interval).

Time frame: Days 91 to 365 post-ablation

Secondary Outcomes

Number of participants with complications

Composite safety endpoint composed of: * cardiac tamponade requiring drainage * persistent phrenic nerve palsy lasting \>24 hours * serious vascular complications requiring intervention * stroke/TIA * atrioesophageal fistula * death

Time frame: Days 0 to 30 post-ablation

Total procedure time

Procedural endpoint

Time frame: Day 0

Total left atrium indwelling time

Procedural endpoint

Time frame: Day 0

Total fluoroscopy time

Procedural endpoint

Time frame: day 0

Total radiation dose

Procedural endpoint

Time frame: Day 0

Contrast agent usage

Procedural endpoint

Time frame: Day 0

Increase in hsTroponin on day 1 post-ablation

Procedural endpoint

Time frame: Day 1

Proportion of isolated veins

Assessed by post-ablation 3D electro-anatomical mapping in the first 25 patients in each study group

Time frame: Day 0

Proportion of isolated carinas

Assessed by post-ablation 3D electro-anatomical mapping in the first 25 patients in each study group

Time frame: Day 0

Lesion size

Assessed by post-ablation 3D electro-anatomical mapping in the first 25 patients in each study group

Time frame: Day 0

Time to first recurrence of atrial tachyarrhythmia between days 1 and 90 after ablation

Time to first recurrence of any atrial tachyarrhythmia (atrial fibrillation \[AF\], atrial flutter \[AFL\] or atrial tachycardia \[AT\]) between days 1 and 90 post ablation as detected on continuous implantable cardiac monitor (ICM). AF, AFL or AT will qualify as a recurrence after ablation if it lasts 120 s or longer on ICM (the minimum programmable episode interval).

Time frame: Days 1 to 90 post-ablation

Arrhythmia burden evaluated based on continuous ICM (overall AF burden = % time in AF)

Assessed by the ICM Core Lab post implantation: between 0-90 days; 91-365 days, 365 days to explantation/end of life of the ICM

Time frame: Between: 0-90 days, 91-365 days, 365 days up to 3.5 years

Arrhythmia being AF or organized atrial arrhythmias (atrial flutter or atrial tachycardias)

Comparison of the prevalence of the type of arrhythmia recurrences during follow-up being AF or organized atrial arrhythmias (AFL or AT)

Time frame: 3, 12, 24 and 36 months follow up

Average heart rates

Average heart rates in ICM documentation in months 1, 2 and 3 after ablation

Time frame: Months 1, 2 and 3 post-ablation

Proportion of patients admitted to the hospital or emergency room because of documented recurrence of atrial arrhythmias

Based on telephone follow-up

Time frame: Postablation 3 months (+/- 2 weeks), 12 months (+/- 2 months), 24 months (+/- 2 months) and 36 months (+/- 2 months)

Proportion of patients undergoing electrical cardioversion because of documented recurrence of atrial arrhythmias

Based on telephone follow-up

Time frame: Postablation 3 months (+/- 2 weeks), 12 months (+/- 2 months), 24 months (+/- 2 months) and 36 months (+/- 2 months)

Proportion of patients undergoing a repeat ablation procedure because of documented recurrence of atrial arrhythmias

Based on telephone follow-up

Time frame: Postablation 3 months (+/- 2 weeks), 12 months (+/- 2 months), 24 months (+/- 2 months) and 36 months (+/- 2 months)

Reinitiation of antiarrhythmic drugs during follow-up

Reinitiation of antiarrhythmic drugs during follow-up based on telephone follow-up

Time frame: Months 3, 12, 24 and 36 post-ablation

Number of reconnected veins evaluated during redo-procedures

Time frame: During redo-procedure, expected to be on average 20-60 minutes

Evolution of Quality of Life through months 3 and 12

QoL questionnaires (EQ-5D) will be sent to the patients by mail after 3 and 12 months to compare the evolution of QoL after the ablation

Time frame: Months 3 and 12 post-ablation

Stroke including TIA after 3, 12, 24 and 36 months

Time frame: Months 3, 12, 24 and 36 post-ablation

Death cardiovascular or non-cardiovascular after 3, 12, 24 and 36 months

Time frame: Months 3, 12, 24 and 36 post-ablation

Sites (anatomical location) of vein reconnection assessed in study patients undergoing a Redo-Procedure at one of the study centres

Time frame: During redo-procedure, expected to be on average 20-60 minutes

Size (area calculate in cm2) of antral scar area assessed in study patients undergoing a Redo-Procedure at one of the study centres

Time frame: During redo-procedure, expected to be on average 20-60 minutes

SINGLE SHOT CHAMPION

Overview

Conditions

Interventions

Eligibility

Locations (2)

Outcomes

Primary Outcomes

Secondary Outcomes