NL-OMON25330尚未招募不适用
REAL-TIME BEDSIDE MONITORING OF BLOOD PROPOFOL CONCENTRATIONS: <br>Comparison between propofol 2% and propofol 1%
niversitair Ziekenhuis BrusselLaarbeeklaan 101 1090 Jette0 个研究点目标入组 24 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 24
研究概览
简要总结
/A
研究设计
- 研究类型
- Observational
入排标准
入选标准
- •Male and female non-pregnant patients scheduled for elective intracranial surgery, ear surgery or thyroid surgery with a minimal duration of at least 3 hours.
- •ASA Physical status I or II
排除标准
- •Serious impairment of respiratory, cardiovascular, hepatic, renal, haematopoetic or endocrine function.
- •Known allergy to propofol or constituents (Soya-bean-eggs).
研究者
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