jRCT1031230452招募中不适用
Sugammadex dosing based on ideal or actual body weight in underweight patients.
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 32
- 主要终点
- -
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
- Randomized Controlled Trial
- 干预模型
- Parallel Assignment
- 主要目的
- Treatment Purpose
- 盲法
- Single Blind
入排标准
- 年龄范围
- 20age old over 至 No limit（—）
- 性别
- All
入选标准
- •BMI below 18.5
- •ASA-PS= 1-3
排除标准
- •ppatient who is allergic to muscle relaxants
- •patient who has neuromuscular diseases
- •patient who has moderate to severe liver function failure
- •Patients with hypoalbuminemia
- •Patients taking medications that affect the muscle relaxant effect
- •Patients who are deemed inappropriate as research subjects by the principal investigator
结局指标
主要结局
-
Time from sugammadex administration to TOFR=90%.
次要结局
未报告次要终点
研究者
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