Background and Aim: Cold snare polypectomy (CSP) is a standard treatment for small colorectal polyps. This study examined the effect of different snare wire diameters on complete histological resection rate, resection depth, and CSP safety. Methods: This randomized controlled trial was conducted at two institutions between June 2019 and March 2021. Eligible colorectal polyps (≤10 mm) were randomly assigned in a 1:1 ratio to receive either CSP with a conventional snare made of normal-diameter wire (0.40 mm) or CSP with a dedicated snare made of thin wire (0.23 mm). The primary endpoint was the complete resection rate determined on histological assessment of the resected specimen. Results: In total, 254 lesions in 152 patients were included, with 128 and 126 lesions assigned to the normal-diameter wire snare group and the thin-wire snare group, respectively. No significant differences were observed in patient characteristics between the two groups. The histological complete resection rate was significantly higher in the thin-wire snare group than in the normal-diameter wire snare group (70.0% vs 81.0%, P = 0.04). The normal-diameter wire snare group had significantly more cases of unclear horizontal margin evaluation than the thin-wire snare group (28.1% vs 15.9%, P = 0.02). No significant differences were observed between the two groups in the muscularis mucosa and submucosa of the resected specimens or the thickness of the submucosa in the resected specimens. Conclusions: CSP with a dedicated thin-wire snare provides more specimens that can be evaluated at the horizontal end and increases the histological complete resection rate. maceutical Co. T.G. received honoraria for his lectures from FUJIFILM Co., FUJIFILM Medical Co., Olympus Co. AstraZeneca K. K., Daiichi Sankyo Co., MC Medical, Inc., and AMCO Co. Author contributions: S.S. and T.H. proposed the study. S.S., T.H., and C.K. performed the research. A.S. and M.Y. performed the pathological examination. T.H. conducted the statistical analysis. T.H. and S.S. wrote the first draft. H.I. and T.G. critically revised the manuscript for important intellectual content.
Ethics statement:The study protocol was approved by the institutional review board at Yuri Kumiai General Hospital on May 28, 2019, and was approved by each participating institution. Written informed consent was obtained from all patients before enrolment. Funding sources: None.