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临床试验/NCT06236282
NCT06236282已完成不适用

Safety and Efficacy of Flexible Articulated Instrument (ArtiSential®) in Laparoscopic Surgery for Rectal Cancer

Seoul National University Hospital1 个研究点 分布在 1 个国家目标入组 93 人开始时间: 2012年5月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
93
试验地点
1
主要终点
Operation time

研究概览

简要总结

This study aimed to assess efficacy of ArtiSential® in reducing laparoscopic rectal cancer surgery duration. We retrospectively reviewed the data of patients who underwent laparoscopic low or ultralow anterior resection for primary mid-to-low rectal cancer, performed by a single surgeon in 2012-2022. Patients were divided into groups, use group vs. non-use group, based on the use or non-use of the ArtiSential®. The total mesorectal excision quality and resection margin status did not differ between the groups. ArtiSential® reduced operative time without impairing surgical quality or oncologic outcomes.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

性别
All
接受健康志愿者

入选标准

  • mid-to-low rectal caner (witing 10cm of the anal verge)
  • laparoscopic surgery

排除标准

  • combined surgery
  • recurrent rectal cancer surgery

结局指标

主要结局

Operation time

时间窗: 0 week

To determine whether the use of articulated device can shorten total operative time

次要结局

  • TME quality (Operative outcome)(0 weeks)
  • Long-term Survival(2 year)
  • Anastomotic leakage (postop outcome)(4 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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