TCTR20211102001已完成2 期
Intrauterine Misoprostol Combined with Oxytocin for Reducing Blood Loss during Cesarean Delivery
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 333
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
- 15 Years 至 45 Years（—）
- 性别
- Female
入选标准
- •inpatient department of OB-GYN unit who indicated for cesarean section.
排除标准
- •Our patients no contraindication for administrated misoprostol
- •The patient who reported co-morbid diseases of bleeding tendency
研究者
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