IRCT20120915010841N21招募中2 期
Comparative Evaluation of intravenous Propofol and Midazolam on sedation and nausea & vomiting during spinal anesthesia in cesarean section
适应症
试验速览
- 阶段
- 2 期
- 状态
- 招募中
- 入组人数
- 102
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
- 18 years 至 46 years（—）
- 性别
- Female
入选标准
- •18-45 aged pregnant women for C/S
- •ASA CLASS 1, 2
- •Satisfaction to participate in the project
- •Pregnant women who underwent cesarean section under spinal anesthesia
排除标准
- •sensitivity to medications used
- •Patients who have failed spinal anesthesia and undergo general anesthesia
- •Lung disease, heart disease, asthma, fever, hypertension, preeclampsia and eclampsia, cardiac arrhythmia
- •Emergency Cesarean
- •Eclampsia and Preeclampsia
- •Multiple pregnancy
- •Spinal anesthesia contraindications (high ICP, hypovolemia, anemia, coagulation disorders, etc.)
- •History of allergy to eggs, soy, midazolam and propofol
- •Use of antiemetic drugs
研究者
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