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临床试验/IRCT20220116053734N1
IRCT20220116053734N1招募中3 期

Evaluation of the effect of paracetamol with Entonox in comparison with pethidine with Entonox on labor pain

Qazvin University of Medical Sciences0 个研究点目标入组 100 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
招募中
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 45 years(—)
性别
Female

入选标准

  • Patients should be between 18 and 45 years old.
  • The fetal presentation should be cephalic.
  • Fetuses are single.
  • Dilatation of the uterus should be 4 cm.

排除标准

  • Having a fetal growth disorder
  • Having a history of chronic pain
  • Having an addiction to drugs, alcohol and smoking
  • Having indications for cesarean section
  • Havind a history of severe psychological disorders, cardiovascular, renal, respiratory, asthma, diabetes, hypertension, coagulation disorders and epilepsy in mother

研究者

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