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临床试验/PACTR201803003123163
PACTR201803003123163已完成未知

Obstetric outcomes following immedicate versus delayed intravenous Oxytocin after amniotomy among parturients: A randomized clinical trial

Kenyatta National Hospital0 个研究点目标入组 202 人开始时间: 2018年2月20日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
202

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 Year(s) 至 45 Year(s)(—)
性别
Female

入选标准

  • Pregnant mothers who:
  • 1.Provide informed consent
  • 2.Have intact membranes at 37 completed weeks or greater.
  • 3. Have singleton vertex pregnancies.
  • 4.Require ARM (at cervical dilatation of 4 cm) for example due to inadequate uterine contractions or poor progress in labour.

排除标准

  • Pregnant mothers in labour with:
  • 1.Multiple gestation.
  • 2.Malpresentation (non-vertex)
  • 3.Previously had uterine surgery.
  • 4.Virally unsuppressed HIV infection.
  • 5.Non-reassuring fetal status prior to amniotomy.
  • 6.Post amniotomy meconium stained liquor, fetal tachycardia, fetal bradycardia, umbilical cord or limb prolapse.
  • 7.Antepartum hemorrhage due to any cause.
  • 8.Hypertensive disease, Diabetes and Cardiac disease in pregnancy.
  • 9.Known/ suspected fetal growth restriction.
  • 10.Parity > 5 (grand multipara)

研究者

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