NCT00660413已完成4 期
Comparison of Acceleromyography and Mechanomyography for Establishing Potency of Neuromuscular Blocking Agents, A Randomized Controlled Study
适应症
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 入组人数
- 40
- 试验地点
- 2
- 主要终点
- Comparison of ED50 with the two methods
研究概览
简要总结
The purpose of this study was to compare two methods for neuromuscular monitoring, acceleromyography and mechanomyography for establishing the dose-response relationship and the potency of a neuromuscular blocking agent using rocuronium as an example. We hypothesized that there would be no significant difference between potencies estimated using acceleromyography and mechanomyography.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 主要目的
- Treatment
- 盲法
- Single
入排标准
- 年龄范围
- 18 Years 至 65 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •ASA I-III
- •Ideal weight +/-20%
- •Both arms available for neuromuscular monitoring
- •Surgery in supine position
- •Participated surgery time more than 30 min
排除标准
- •Pregnant and breast-feeding women
- •Patients with known illness or use of medications known to influence the neuromuscular transmission
- •Known significant renal or hepatic dysfunction
- •Allergy to medications used in the study
结局指标
主要结局
Comparison of ED50 with the two methods
次要结局
- Comparison of ED95 with the two methods
研究者
研究点 (2)
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