Aims Duodenal mucosal ablation (DA) is a promising endoscopic treatment for metabolic disease including T2D. A multitude of technologies are in development; however, limitations exist around usability, ablation uniformity, and adverse events. Vapor ablation, using the FDA cleared Aqua Medical RFVA system, is an emerging therapy that could be used for DA. Proof-of-concept data in Barrett's esophagus has established its safety and technical feasibility [1]. We aimed to evaluate the safety and utility of RFVA in the duodenum in a porcine dosimetry pre-clinical study.
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Norton et al. (2024) studied this question.
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