Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/56872
Title: First-In-Human Study to evaluate the safety and feasibility of EnCompass-S2 ARFA PFA (Advanced Radiofrequency Ablation Pulsed Field Ablation) Dual Energy Clamp in patients undergoing cardiac ablation during a concomitant cardiac surgical procedure. (EnCompass-S2 FIH)
Monash Health Investigator(s): Bennetts J.
Monash Health Department(s): Cardiology (MonashHeart)
Registration Date: 24-Jul-2025
Monash Health Site(s): Victorian Heart Hospital
Trial Phase: Not Applicable
Summary: Atrial fibrillation (AF) is the most common sustained cardiac arrhythmia worldwide. Surgical ablation for the treatment of AF during concomitant cardiac surgery is a class I recommendation per Society of Thoracic Surgeons (STS) and Heart Rhythm Society (HRS) guidelines. The AtriCure Isolator Synergy EnCompass-S ARFA PFA Dual Energy Ablation System will be used to treat AF as part of planned cardiac surgery. The objective of this study is to evaluate the safety and feasibility of the Isolator Synergy EnCompass-S2 AFRA PFA Dual Energy System in participants with atrial fibrillation (AF) undergoing cardiac ablation concomitant to cardiac surgery.
Type: Clinical trial
Registry ID: ACTRN12625000778482
URL: https://www.anzctr.org.au/Trial/Registration/TrialReview.aspx?id=389945
Appears in Collections:Clinical Trials

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