IRCT20240713062414N1招募中3 期
Efficacy of vaginal cleansing in reducing postoperative infection after Cesarean Delivery
适应症
试验速览
- 阶段
- 3 期
- 状态
- 招募中
- 入组人数
- 205
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
- no limit 至 no limit（—）
- 性别
- Female
入选标准
- •All woman with cesarean indications
- •Obtaining informed consent to enter the study
排除标准
- •Women with chorioamnionitis
- •Allergy for povidon iodine
- •Vaginal bleeding from placenta previa
- •Active genital herpes
研究者
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