KCT0001502已完成未知
Comparison of predictive performance between modified Marsh propofol model and Schnider propofol model in underweight patients
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 30
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional Study
入排标准
- 年龄范围
- 20(Year) 至 o Limit（—）
- 性别
- All
入选标准
- •1. body mass index (BMI) < 18.5 (kg/m2)
- •2. Hemoglobin > 9 (mg/dl)
- •3. Patients undergoing elective surgery under general anesthesia
排除标准
- •1. Pregnant or nursing (lactating) women, where pregnancy is defined as the state of a female after conception and until the termination of gestation, confirmed by a positive urine pregnancy test
- •2. Patients with known hypersensitivity to propofol or to any of the excipients
- •3. Clinically significant impairment of cardiovascular, respiratory and renal function
- •4. Patients who are considered by the investigator to be unsuitable to participate in the study for any other reason not mentioned in the inclusion and exclusion criteria.
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