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临床试验/IRCT20120215009014N455
IRCT20120215009014N455招募中3 期

Comparison of the effect pethidine, paracetamol and their combination on the reduction of labor pain and the level of satisfaction of primiparous women

Hamedan University of Medical Sciences0 个研究点目标入组 111 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
招募中
入组人数
111

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 40 years(—)
性别
Female

入选标准

  • Age of 18 to 40 years
  • Term pregnancy
  • A singleton with a cephalic display
  • Cervical dilatation 4 cm
  • Pregnant women undergoing induction of labor with oxytocin

排除标准

  • Analgesic consumption in the last 24 hours
  • Preeclampsia and eclampsia
  • Severe obesity
  • Intrauterine fetal death
  • Fetal abnormalities

研究者

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