NCT02575443已完成不适用
Neuromuscular Block and Anesthetic Depth Monitoring
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
- 60
- 试验地点
- 1
- 主要终点
- Total infused dose of propofol
研究概览
简要总结
The purpose of this study is to evaluated whether the depth of neuromuscular block may affect the unicon value of anesthetic depth monitoring system (ADMS).
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Diagnostic
- 盲法
- None
入排标准
- 年龄范围
- 20 Years 至 80 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Gall bladder disease
- •American Society of Anesthesiologist physical status 1 or 2
排除标准
- •Pregnancy
- •Body mass index < 16
- •Body mass index >30
- •Neuromuscular disease
- •Previous intraabdominal surgery
研究组 & 干预措施
Moderate block (MB) group
Experimental
干预措施: Rocuronium (MB group) (Drug)
Deep block (DB) group
Experimental
干预措施: Rocuronium (DB group) (Drug)
结局指标
主要结局
Total infused dose of propofol
时间窗: At 1 min after the anesthesia is finished
次要结局
- Electromyographic index presented on the anesthetic depth monitoring system(Through study completion, an average of 2 hours)
研究者
Hyo-Seok Na
Dr
Seoul National University Bundang Hospital
研究点 (1)
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