EUCTR2005-002812-94-GB进行中（未招募）1 期
Randomised trial of carbetocin versus oxytocin for the prevention of postpartum haemorrhage after caesarean section - LOXY Trial
orth Bristol NHS Trust0 个研究点目标入组 380 人开始时间: 2005年6月29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
- 380
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
入选标准
- •Women undergoing elective or emergency caesarean section after 37 weeks of pregnancy.
- •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
- •Women with multiple gestation, placenta praevia and placental abruption.
- •Women undergoing caesarean section with general anaesthesia.
- •Women with caesarean section at less than 37 weeks.
- •Women having emergency caesarean section for fetal or maternal distress.
研究者
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