跳至主要内容
临床试验/NCT02267551
NCT02267551终止不适用

Non-inferiority Study Comparing daVinci Skills Simulator to Mimic dV-Trainer for Preparing Residents to Perform Live Human Surgery

Atlantic Health System1 个研究点 分布在 1 个国家开始时间: 2014年4月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
终止
试验地点
1
主要终点
Operative Time

研究概览

简要总结

The objective of this study is to determine whether a group of resident physicians otherwise naïve to robotic surgery can demonstrate equal levels of proficiency during their first robotic supracervical hysterectomy having received training either with the Mimic dV-Trainer or the daVinci Skills Simulator.

研究设计

研究类型
Interventional
分配方式
Randomized
主要目的
Health Services Research

入排标准

性别
All
接受健康志愿者
否

入选标准

  • •Obstetrics and gynecology or general surgery residents in ACGME accredited programs naïve to robotic surgery training
  • •Completion of the online orientation to daVinci Surgical System

排除标准

  • •Performance of any robotic surgical procedures as the console surgeon
  • •Performance of any robotic simulator protocols
  • •Any significant amount of time spent on a virtual reality robotic simulator

研究组 & 干预措施

Mimic dV-Trainer

Other

干预措施: Mimic dv-Trainer (Other)

daVinci Skills Simulator

Other

干预措施: daVinci Skills Simulator (Other)

结局指标

主要结局

Operative Time

时间窗: at time of supracervical hysterectomy

Operative time will be measured by time elapsed between first grasp of the uterine fundus with the robotic single tooth tenaculum until amputation of the specimen at the internal cervical os.

次要结局

  • Estimated Blood Loss(during the surgical procedure)
  • Surgical Skill Rating(following completion of the procedure)
  • Continued success with robotic surgery after participation in the study(during the 12 months following surgical procedure)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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