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