NL-OMON36134已完成不适用
Population PK/PD of propofol and nadroparin in extreme morbidly obese patients - POP4 study
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 8
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 至 99（—）
入选标准
- •8 morbidly obese patients a total body weight higher than 170 kg undergoing laparoscopic banding, laparoscopic sleeve gastrectomy or gastric bypass surgery, with a Body Mass Index > 40 kg/m2, 18-60 year old and American Society of Anaesthesiologists (ASA) physical status II to III.
排除标准
- •Epilepsy, pregnancy, breastfeeding and known allergy for propofol, nadroparin, egg lecithin or soy bean oil.
研究者
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