ISRCTN14718882已完成未知
Intramuscular oxytocin versus intravenous oxytocin to prevent haemorrhage at vaginal delivery - A randomised controlled trial
Coombe Women and Infants University Hospital0 个研究点目标入组 1,000 人开始时间: 2016年1月4日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 1,000
研究概览
简要总结
2017 protocol in: https://www.ncbi.nlm.nih.gov/pubmed/29141679 2018 results in: https://www.ncbi.nlm.nih.gov/pubmed/30181338 [added 20/03/2019]
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- Female
入选标准
- •1. Aged 18 or over
- •2. Female participants only
- •3. Singleton pregnancy at more than 36 weeks gestation
- •4. Those anticipated to have a vaginal delivery
排除标准
- •1. Women who opted for physiological management of the third stage of labour
- •2. Those who have an antenatal decision for 40IU oxytocin infusion prophylactically following a vaginal delivery
- •3. Those whom the clinician has a preferred route of administering prophylactic oxytocin for the third stage of labour
- •4. Those who are deemed to be at risk of postpartum haemorrhage - Previous history of atonic primary postpartum haemorrhage, multiple fibroids, coagulation disorders, thrombocytopenia and receiving anticoagulants
- •5. Those with previous cardiovascular disorder
研究者
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