NCT02762890已完成不适用
Comparison of Deep Neuromuscular Block and Moderate Neuromuscular Block on Quality of Recovery in Patients Undergoing Robotic Gastrectomy
适应症
干预措施
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 56
- 试验地点
- 1
- 主要终点
- Postoperative quality of recovery
研究概览
简要总结
The purpose of this study is to investigate and compare the postoperative quality of recovery between the deep neuromuscular blockade and moderate neuromuscular blockade during robotic gastrectomy.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Prevention
- 盲法
- Double (Participant, Outcomes Assessor)
入排标准
- 年龄范围
- 19 Years 至 80 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •adult patients aged 19-80 years who are scheduled for robotic gastrectomy
排除标准
- •Neuromuscular disease
- •History of malignant hyperthermia
- •Significant renal or hepatic dysfunction
- •Allergy to sugammadex or rocuronium
研究组 & 干预措施
Deep neuromuscular blockade
Experimental
Rocuronium will be administered continuously to achieve post-tetanic count 1-2 during surgery.
干预措施: Deep neuromuscular blockade (Drug)
Moderate neuromuscular blockade
Active Comparator
Rocuronium will be administered continuously to achieve Train-of-four 1-2 during surgery.
干预措施: Moderate neuromuscular blockade (Drug)
结局指标
主要结局
Postoperative quality of recovery
时间窗: within 48 hours after the end of surgery.
The postoperative quality of recovery will be evaluated at 24 and 48 hours after the end of surgery by the investigator who are blinded to the group assignments.
次要结局
- Surgical condition(within 48 hours after the end of surgery)
- shoulder pain(within 48 hours after the end of surgery)
- abdominal pain(within 48 hours after the end of surgery)
- nausea and vomiting(within 48 hours after the end of surgery)
研究者
研究点 (1)
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