KCT0003501已完成不适用
Comparison of perfusion index in response to noxious stimulation under monitored anesthesia care: propofol / remifentanil vs propofol / dexmedetomidine
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 76
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational Study
入排标准
- 年龄范围
- 19(Year) 至 70(Year)（—）
- 性别
- All
入选标准
- •American Society of Anesthesiologist (ASA) class I, II Adult
排除标准
- •Pediatric patients Patients with American Society of
- •Anesthesiologist (ASA) class III, IV Patients with a Body mass index (BMI)
- •greater than 30 Diabetes Peripheral obstructive blood vessel disease Patients
- •with heart disease (myocardial infarction, heart failure, arrhythmia) Patients
- •who is taking a / ß blocker pregnancy Anyone who is allergic to certain
- •anesthetics or drugs due to a history (propopol related allergy or history:
- •previous hypersensitivity reactions, hypersensitivity to soy or peanuts)
- •bradycardia (HR < 50 bpm) Chronic pain disorder Severe liver, kidney
研究者
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