IRCT20220430054707N1尚未招募3 期
comparison of the effect of intravenous and subcutaneous Dexamethasone on prevention of pain after caesarian section
适应症
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 入组人数
- 156
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 45 years（—）
- 性别
- Female
入选标准
- •Candidate for non-emergency cesarean section
- •Not having allergy to dexamethasone
- •Age between20-45
- •Not having contraindications to spinal anesthesia
排除标准
- •Prolongation of cesarean section more than 2 hours
- •Convert spinal anesthesia to general for any reason.
研究者
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