Dual-energy ablation
Clinical evidence
Sphere-9™ catheter clinical evidence for ventricular tachycardia (VT)
CAUTION: The use of the Sphere-9™ catheter for VT ablation and the associated software are investigational in Europe. This evidence has not been evaluated yet.
Exclusively integrated with Affera™ mapping and ablation system
All-in-one: mapping, radiofrequency (RF) and pulsed field ablation (PFA) catheter
Wide-area focal ablation catheter
Tissue-conformable lattice tip
Pulsed field mapping to verify VT ablation targets at critical locations
The Sphere-9™ Ventricular Tachycardia Early Feasibility Study (EFS) is a prospective, multicenter, nonrandomized feasibility study designed to evaluate the safety and performance of the Sphere-9™ catheter integrated with the Affera™ mapping and ablation system. The study evaluates investigational RF and PFA therapy settings for the treatment of recurrent, sustained, scar-related monomorphic VT. The study was initiated to include patients with ischemic cardiomyopathy only, and enrollment began in March 2025. The trial was expanded to included nonischemic cardiomyopathy patients in 2026. A U.S. pivotal trial (Sphere VT) was approved to begin enrollment in April 2026.
The study is a prospective EFS designed to evaluate the safety and performance of the Affera™ ablation system using the Sphere‑9™ catheter for the treatment of monomorphic VT due to prior myocardial infarction.
100%
primary
effectiveness
Acute noninducibility of the
clinically relevant VT (N = 40)
0
burden
post-ablation
Median device detected VT episodes
per month post-ablation (N = 20)
65.5%
freedom from
any sustained
monomorphic VT
Interim Kaplan-Meier estimate;
follow-up ongoing for 20/40 patients
† N = device-related safety events reported in 2/40 patients.
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