Ventricular tachycardia (VT) is alife-threatening arrhythmia originating from the heart's ventricles. Traditional treatments include antiarrhythmic medications, implantable cardioverter-defibrillators (ICDs), and catheter ablation. Stereotactic body radiation therapy (SBRT) targeting the arrhythmogenic focus in the left ventricle-stereotactic arrhythmia radioablation (STAR)-is an emerging treatment and may offer apotential solution for patients with refractory VT. We designed an interventional prospective clinical trial in Israel aligned with the STOPSTORM.eu consortium's benchmarks, recommendations, and directives to assess the safety and efficacy of STAR in patients with refractory VT. Our phaseI/II single-institutional trial was approved by the Ministry of Health of Israel for 10patients, initially assessing safety in the first 3patients. We included patients with ICDs experiencing symptomatic monomorphic VT after an inadequate response to previous therapies. The primary endpoints were treatment-related serious adverse events and areduction in VT burden as assessed by ICD interrogation. Secondary outcomes included areduction in antiarrhythmic medications and changes in quality of life. From August 2023 to August 2024, 3patients underwent STAR treatment. The prescription dose was asingle fraction of 25 Gy. Planning target volumes were 47.8, 49.7, and 91.8 cc, and treatment was successfully delivered with no grade3 or higher adverse events reported. Over afollow-up period of 12months for the first patient and 8months for the second one, no VT events were recorded after treatment. The third patient died from progressive heart failure 3months after treatment. Left ventricular ejection fraction remained stable, and no significant radiation-induced inflammatory changes were noted. The initial results of this trial suggest that STAR can reduce VT episodes in patients with refractory VT without severe adverse effects. The study highlights the importance of international collaboration and standardization in pioneering new treatments. Further follow-up and additional patient data will be necessary to confirm these findings and evaluate long-term outcomes, including potential adjustments to antiarrhythmic medication regimens.