EUCTR2007-002341-20-GB进行中（未招募）不适用
Randomized controlled trial comparing the effect of carbetocin vs syntocinon and ergometrine on postpartum haemorrhage in patients undergoing elective caesarean section - C.A.S.E. Trial
Queen Charlotte's and Chelsea Hospital0 个研究点目标入组 600 人开始时间: 2008年5月16日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 600
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
- •Full consent from patient, over 18 years of age
- •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
- •Hypersensitivity to carbetocin or oxytocin, hepatic or renal disease, vascular disease, severe cardiac disease, impaired pulmonary function, sepsis, severe hypertension, pre-eclampsia or eclampsia, contraindications to ergometrine (previous hypersensitivity or idiosyncratic reactions to ergometrine or other ergot alkaloids, current use of doxycycline, tetracycline, sumatriptan, dopamine or methysergide, postpartum use of bromocriptine), general anaesthesia, Patients on erythromycin will be excluded as ergot toxicity can develop rapidly in patients on ergotamine.
研究者
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