This study aims to evaluate the safety and efficacy of new ablation catheter developed by MEDICAL TAEWOONG for the treatment of pancreatic neoplasm (pancreatic adenocarcinoma or neuroendocrine tumour). The ablation is performed using EUSRA needle and radio frequency waves under ultrasound imaging. The subject who will be recruited into this study are patients who are deemed as non-surgical candidates.
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To measure the technical success of EUS-guided RFA
Timeframe: 18 months
To measure side effects and adverse event of EUS-guided RFA
Timeframe: 18 months