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临床试验/TCTR20210914002
TCTR20210914002尚未招募3 期

Efficacy of intramyometrial versus intravenous oxytocin for reduction of blood loss vulume after elective cesarean section; a double blinded randomized controlled trial

Faculty of Medicine Siriraj Hospital0 个研究点目标入组 100 人开始时间: 2021年9月14日最近更新:
适应症

试验速览

阶段
3 期
状态
尚未招募
入组人数
100

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 N/A (No limit)(—)
性别
Female

入选标准

  • 1.pregnant women who came for elective cesarean section at Siriraj Hospital
  • 2.gestational age at 34 weeks or more

排除标准

  • 1. In active phase if labor
  • 2. Hematologic disorder that effect bleeding tendency
  • 3. Contraindication for oxytocin
  • 4. Allergy to oxytocin or its composition
  • 5.Obstetric condition that risk for bleeding such as placenta previa, preeclampsia
  • 6.Fetal anomalies
  • 7. Fetal death
  • 8. Conduct general anesthesia for Cesarean section

研究者

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