PACTR201505001107182已完成未知
COMPARATIVE EFFECTIVENESS OF 200µG VERSUS 400µG OF SUBLINGUAL MISOPROSTOL FOR THE PREVENTION OF PRIMARY POSTPARTUM HAEMORRHAGE: A RANDOMISED CONTROLLED TRIA
Dr I.A Ugwu0 个研究点目标入组 0 人开始时间: 2015年4月16日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
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 45 Year(s)（—）
- 性别
- Female
入选标准
- •Women at term with singleton pregnancy in active phase labour, or
- •women undergoing induction of labour and with anticipated spontaneous vaginal delivery
排除标准
- •contraindications for use of misoprostol such as asthma
- •paturients undergoing caesarean section
- •presence of coagulation disorders
- •pre-eclampsia and other hypertensive diseases in pregnancy
- •conditions requiring prophylactic oxytocin infusion after delivery such as grandmultiparity, multiple pregnancy, polyhydramnios and coexisiting uterine fibroids
- •previous history of postpartum haemorrhage
- •history of anteparturm haemorrhage
- •Refusal or withdrawal of consent
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