EUCTR2018-001829-11-GB进行中（未招募）1 期
The Carboprost or Oxytocin Postpartum haemorrhage Effectiveness Study. Carboprost vs Oxytocin as the First Line Treatment of Primary Postpartum Haemorrhage; A phase IV, double-blind, double-dummy, randomised controlled trial. - COPE
niversity of Liverpool0 个研究点目标入组 3,948 人开始时间: 2019年11月12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
- 3,948
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
- •= 16 years of age
- •Requirement for medical treatment for primary PPH
- •Are the trial subjects under 18? yes
- •Number of subjects for this age range: 198
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 3750
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Known to have opted out of participation antenatally
- •Known oxytocin or carboprost hypersensitivity
- •Known active cardiac or pulmonary disease
- •Known to have previously been treated as part of COPE
- •Has already received carboprost prophylactically for postpartum haemorrhage
- •Has already received uterotonic drug treatment for postpartum haemorrhage (this does not include PPH prophylaxis)
研究者
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