TCTR20160715004已完成未知
Efficacy of intravenous 100 mcg carbetocin versus intravenous 5 units oxytocin for prevention of immediate postpartum hemorrhage after normal vagina delivery among high risk prenancies; a tripple-blinded randomized controlled trial
Siriraj Routine to Research Unit0 个研究点目标入组 350 人开始时间: 2016年7月15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
- 350
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 20 Years 至 50 Years（—）
- 性别
- Female
入选标准
- •1. Thai pregnant woman
- •2. age at least 20 years old
- •3. Pregnancy age at least 34 weeks gestation
- •4. normal vaginal delvery
- •5. high risk for PPH including previous history of PPH, induction or augmentation of labour, tocolytic drug before delivery, prolonged active phase of labour, precipitate labour, grand multipara, overdistended uterus, uterine structural abnormality
排除标准
- •1. being active labour
- •2. Contraindication to carbetocin
- •3. allergy to oxytocin or carbetocin
- •4. obstetrics complication including preeclampsia and abnormal placentation
研究者
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