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临床试验/TCTR20120000012
TCTR20120000012已完成4 期

Comparison of postpartum blood loss between intravenous oxytocin and intravenous methylergometrine maleate during third stage of labor

Department of Obstetrics and Gynecology, Faculty of Medicine Ramathibodi Hospital.0 个研究点目标入组 80 人开始时间: 2012年8月6日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
80

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
18 Years 至 34 Years(—)
性别
Female

入选标准

  • 1. Parturients who had normal vaginal delivery
  • 2. Singleton pregnancy
  • 3. Gestational age 37-41 weeks
  • 4. Newborn birth weighed equal or greater than 2500 grams with Apgar score at 1, 5 minutes equal or greater than 7.

排除标准

  • Parturients who had complications during pregnancy and were hypersensitive to oxytocin and/or ergometrine.

研究者

发起方
Department of Obstetrics and Gynecology, Faculty of Medicine Ramathibodi Hospital.

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