ACTRN12618002039268尚未招募未知
Comparison of two electromyographic devices to assess recovery from neuromuscular blockade (muscle relaxants) in patients undergoing general anaesthesia in the operating theatre.
The Sydney Adventist Hospital0 个研究点目标入组 35 人开始时间: 2018年12月20日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 发起方
- 入组人数
- 35
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Prevention
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- All
入选标准
- •Inclusion criteria - 18 years of age, receive neuromuscular blocking agent.
排除标准
- •Exclusion criteria – previous procedures or pre-existing condition where TOF ratio may not be measure accurately, allergy to adhesive gel electrodes, difficult access to the hand, neuromuscular disease.
研究者
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