IRCT20151221025641N5招募中3 期
Comparing the effectiveness of propofol-remifentanil with propofol-dexmedetomidine in reducing pain after awake craniotomy surgery
适应症
试验速览
- 阶段
- 3 期
- 状态
- 招募中
- 入组人数
- 64
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 20 years 至 50 years（—）
- 性别
- All
入选标准
- •The patient should be a candidate for craniotomy surgery using the sleep-awake-asleep method;
- •The patient does not have a previous craniotomy history;
- •The patient does not have a contraindication for full anesthesia;
- •The patient's age is between 20 and 50 years;
- •The patient does not have a history of allergy to any of the drugs under study.
排除标准
- •In addition to craniotomy, the patient needs to perform another surgery at the same time;
- •Breast feeding;
- •The patient has simultaneously heart, renal or liver failure;
- •Severe obesity (BMI>30 kg/m2);
研究者
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