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RCT Comparing Reduced-port Robotic and Conventional Laparoscopic Subtotal Gastrectomy

Yonsei University · 2026
ClinicalTrials.gov · Datasets · License: Public Domain · 2026
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gastric-cancerrobotic-surgery
"Study objective The objective of this study is to evaluate whether reduced-port robotic subtotal gastrectomy demonstrates non-inferiority in safety, specifically regarding the incidence of postoperative complications, compared to conventional laparoscopic subtotal gastrectomy in patients with early gastric cancer. Additionally, the study aims to assess differences in efficacy between the two surgical approaches as secondary endpoints. Study design overview This study is a multicenter, randomized controlled trial involving patients with early gastric cancer. Participants will be randomly assigned in a 1:1 ratio to either the reduced-port robotic surgery group or the conventional laparoscopic surgery group. Outcomes to be observed over a 30-day postoperative period include the incidence of complications, operative time, blood loss, pain levels, length of hospital stay, and quality of life. Investigational Product/Medical Device Robotic surgical platform Laparoscopic surgical platform Target Sample Size and Rationale The study aims to demonstrate that reduced-port robotic subtotal gastrectomy (experimental group) is non-inferior to conventional laparoscopic subtotal gastrectomy (control group) with respect to the incidence of postoperative complications of grade ≥ 3. Previous studies have reported that the complication rate for minimally invasive subtotal gastrectomy in early gastric cancer is approximately 4%. For the non-inferiority test based on comparison of proportions, the following assumptions were used to calculate the required sample size: * Complication rate in the control group (pC): 4% * Complication rate in the experimental group (pT): 4% * Non-inferiority margin (Δ): 5% * Significance level (α): 2.5% (one-sided) * Statistical power (1-β): 80% * Allocation ratio: 1:1 * Expected dropout rate: 10% Based on these assumptions, the calculated sample size is 242 patients per group. Considering a 10% dropout rate, the adjusted sample size is 269 patients p
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