PACTR202306725476304尚未招募Unknown
A comparison of the efficacy of two and three passes of vaginal cleansing with chlorhexidine or placebo before emergency caesarean section in reducing infectious morbidity
Ese Adigba Onodjohwoyovwe0 个研究点目标入组 162 人开始时间: 2023年5月25日最近更新:
适应症
试验速览
- 阶段
- Unknown
- 状态
- 尚未招募
- 发起方
- 入组人数
- 162
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
- 19 Year(s) 至 44 Year(s)（—）
- 性别
- Female
入选标准
- •Inclusion criteria
- •Pregnant women at 28 weeks gestational age or more with indications for emergency caesarean section who will consent to the study will be recruited.
排除标准
- •Exclusion criteria
- •1. Placental praevia
- •2. Clinical chorioamnionitis
- •3. Allergy or contraindication to Chlorhexidine
- •4. Allergy or contraindication to Ceftriaxone
- •5. Cord prolapse
- •6. Pre-exiting medical conditions such as severe anaemia, uncontrolled DM and HIV with unsuppressed viral load
- •7. Gestational age < 28 weeks
- •8. Caesarean hysterectomy
- •9. Elective caesarean section
研究者
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