Cryotherapy Versus Radiofrequency Ablation for Treatment of Para-hisian Accessory Pathways

University of Sao Paulo General Hospital30 enrolled

Overview

A randomized pilot study to evaluate safety and efficacy endpoints for treatment of para-hisian accessory pathways according to two different strategies of lesion formation. These patients will be divided into 2 groups with different strategies of treatment: group 1 treated with radiofrequency (RF) ablation, group 2 with cryotherapy (CRYO). The primary outcome will be the recurrence rate of accessory pathway conduction after one year of follow-up. Secondary endpoints will be immediate success and rate of permanent atrioventricular (AV) block.

This is a randomized study on the safety and efficacy for percutaneous ablation of para-hisian accessory pathways according to two different modalities: radiofrequency (RF) or cryotherapy. Thirty patients with symptomatic or high-risk para-hisian accessory pathways, documented by previous electrophysiological study (EPS), referred to percutaneous catheter ablation, will be enrolled in this trial. After informed consent, these patients will be randomized in 2 groups with different current established strategies of invasive treatment. Group I: electrophysiological mapping and ablation with radiofrequency (RF) focal lesion formation. Group II: electrophysiological mapping and ablation with cryotherapy (CRYO) focal lesion formation. The primary outcome will be the recurrence rate of accessory pathway conduction after one year of follow-up. Secondary endpoints will be immediate success and rate of permanent atrioventricular (AV) block.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Cardiac Arrhythmias

Eligibility

Sex: ALLMin age: 12 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Patients with para-hisian accessory pathways, diagnosed by electrophysiological study (EPS), with indication of invasive treatment according to current guidelines. Patients should be willing and able to sign an informed consent form, and to undergo all procedures described in both the study protocol and the consent form. Exclusion Criteria: * Previous cryotherapy ablation; * Previous extensive radiofrequency ablation (including aortic cusp mapping); * Age below twelve years; * Severe coagulation disorder; * Pregnancy; * Refusal to participate in the study.

Outcomes

Primary Outcomes

One-year recurrence rate

Recurrence rate of accessory pathway conduction, as assessed by follow-up Clinical recording and event monitoring external device (Holter/Looper).

Time frame: One year

Secondary Outcomes

Immediate success rate

Mensuration of immediate success at the EP lab after ablation therapy is finished, defined by elimination of accessory pathway and/or noninducibility of arrhythmias at the end of procedure, as assessed by standard electrophysiological maneuvers. If an evidence of accessory pathway conduction still remains at the end of procedure it will count as an unsuccessful case. Does not take into account recurrences after the end of procedure, e.g. in the hospital ward before discharge.

Time frame: Time span between vein puncture (start of procedure) and sheath removal (end of procedure), comparing with baseline rhythm

Rate of atrioventricular block

Safety outcome of any permanent atrioventricular (AV) block that occurred immediately after ablation start or during hospital admission.

Time frame: up to 24 hours