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临床试验/TCTR20150820001
TCTR20150820001已完成未知

Prevention of Postpartum Hemorrhage with Oxytocin versus Ergometrine Plus Oxytocin in the third stage of labor

Vajira Institutional Review Board0 个研究点目标入组 323 人开始时间: 2015年8月20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
323

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
13 Years 至 45 Years(—)
性别
Female

入选标准

  • singleton pregnancy at >28 weeks of gestation,
  • cephalic presentation,
  • anticipating a normal spontaneous vaginal delivery

排除标准

  • non -cephalic presentation, multiple pregnancies, polyhydramnios, uterine fibroids, previous postpartum hemorrhage, antepartum hemorrhage, parity greater than four, previous cesarean section, severe anemia (hemoglobin level of ≤ 8 g/dL), coagulopathy, contraindications to the use of ergometrine, estimated fetal birth weight >4000 g, inability to obtain written consent, cesarean section, instrumental delivery

研究者

发起方
Vajira Institutional Review Board

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