PACTR201709002597110尚未招募未知
Effectiveness of Preoperative Vaginal Cleansing with Povidone-Iodine in Post-ceasarean Infectious Morbidity; A Randomized Controlled Trial.
The authors0 个研究点目标入组 180 人开始时间: 2017年9月8日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 发起方
- 入组人数
- 180
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 Year(s) 至 40 Year(s)（—）
- 性别
- Female
入选标准
- •All consenting parturients admitted in FETHA for either elective or emergency caesarean section after 37 completed weeks.
排除标准
- •Refusal of consent.
- •Women with known allergy to topical povidone-iodine
- •Placenta praevia.
- •Cord prolapse
- •Clinical Chorioamnionitis
- •Foul smelling discharge on admission.
- •Women with immunosupression due to HIV/AIDS, Diabetes Miletus or chronic use of steroids.
研究者
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