JPRN-jRCTs032180067已完成未知
A non-inferiority randomized controlled trial to evaluate the efficacy and safety of automated delivery of three anesthetics using a robotic anesthesia system for total intravenous anesthesia with propofol, remifentanil, and rocuronium - A non-inferiority randomized controlled trial of automated delivery of three intravenous anesthetics using a robotic anesthesia system for total intravenous anesthesia
agata Osamu0 个研究点目标入组 60 人开始时间: 2018年12月28日最近更新:
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 60
研究概览
简要总结
We obtained useful criteria to assess the appropriate level of analgesia that satisfies the anesthesiologist by examining in detail the information obtained from the interval when the anesthesiologists judged that the patient was in a stable analgesic state during observation period. As the non-inferiority of AC group was indicated with the revised criteria obtained in this study, our criteria will be appropriate for evaluating the effectiveness of automated-control system in future studies.
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- >= 20age old 至 ot applicable(—)
- 性别
- All
入选标准
- •1.Male and female patients over 20 years old at the time of informed consent
- •2.Patients with ASA physical status of 1, 2, and 3 who are scheduled for surgery under general anesthesia
- •3.Patients who understand the contents of this study and are willing to provide written informed consent for participation in this study
排除标准
- •1.Patients with a history of hypersensitive to propofol, remifentanil, rocuronium or sugammadex.
- •2.Patients who are pregnant or lactating.
- •3.Patients who are determined not to be eligible for participation in this study by the research director.
研究者
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