EUCTR2005-001361-34-GB进行中（未招募）1 期
A randomised controlled trial of oxytocin 5 IU versus oxytocin 5 IU and 30 IU infusion for the control of blood loss at elective caesarean section - pilot study. - caesarean third stage trial
niversity of Dundee0 个研究点目标入组 75 人开始时间: 2005年3月31日最近更新:
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 75
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- Female
入选标准
- •Healthy women at term (> 36 weeks) with a singleton pregnancy booked for an elective caesarean section
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •placenta praevia; multiple pregnancy; known coagulopathy; current anti-coagulant therapy; thrombocytopenia
研究者
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终止
4 期
Does the use of oxytocin in a pulsatile fashion (intermittent boluses), when compared to the use of continuous oxytocin, for the commencement and/or assistance of labour, result in a reduction in the number of caesarean sections that are required?abour (induction of)Labour (induction of)Reproductive Health and Childbirth - Antenatal careReproductive Health and Childbirth - Childbirth and postnatal careReproductive Health and Childbirth - Fetal medicine and complications of pregnancyACTRN12619000588190Darren Lowen200