ACTRN12620000971932尚未招募未知
Effect of vaginal antiseptic prior to Caesarean Section on the rate of Post-Caesarean complications: A blinded randomised controlled trial
Goulburn valley health0 个研究点目标入组 375 人开始时间: 2020年9月28日最近更新:
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 发起方
- 入组人数
- 375
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Prevention
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 16 Years 至 o limit（—）
- 性别
- Female
入选标准
- •Any patients undergoing for either emergency or elective CS that provided voluntary informed consent will be included in the study.
排除标准
- •Patients having signs of chorio, intrapartum pyrexia and other signs of infection will be excluded from the study.
- •Patients who develop intrapartum pyrexia as a result of syntocinon drip, prolonged labour or obstructed labour and provided voluntary informed consent will be included in the study initially. Their placental swabs will be taken for microscopic examination, culture and sensitivity (m/cs). They will be excluded from the study only if their swab results are positive for m/cs.
研究者
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