跳至主要内容
临床试验/IRCT20231025059855N1
IRCT20231025059855N1招募中2 期

Efficacy and safety of lidocaine-prilocaine topical cream (XYLA-P) in reducing the intensity of episiotomy pain in normal vaginal delivery

Tehran University of Medical Sciences0 个研究点目标入组 54 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
招募中
入组人数
54

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
20 years 至 35 years(—)
性别
Female

入选标准

  • Healthy pregnant women with first natural delivery
  • Gestational age between 37 and 41 weeks
  • Episiotomy incision below 5 cm
  • Patient satisfaction

排除标准

  • Heavy bleeding during childbirth
  • The need to use a vacuum during delivery
  • Grade 3 and 4 perineal lacerations
  • History of previous allergy to lidocaine or prilocaine

研究者

相似试验

Topical lidocaine and pain reduction in natural... | 临床试验