ACTRN12612000095864尚未招募1 期
combined Use of Oxytocin and Misoprostol versus oxytocin infusion and Misoprostol alone toreduce blood loss at cesarean section
Qazvin University of Medical Science0 个研究点目标入组 150 人开始时间: 2012年1月19日最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 150
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
- 18 Years 至 42 Years（—）
- 性别
- Female
入选标准
- •pregnant women at term (37—40 wks) gestation scheduled for either elective or emergency lower segment cesarean
排除标准
- •excluding criteria:Women with any risk factor
- •associated with an increased risk of postpartum
- •hemorrhage were excluded i.e. anemia (Hb8 g%), multiple gestation, antepartum hemorrhage,poly-hydramnios, two or more previous cesarean sections and/or a history of previous rupture uterus, current or previous history of significant disease including heart disease, liver, renal disorders or known coagulopathy
研究者
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