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临床试验/IRCT20100130003226N19
IRCT20100130003226N19招募中3 期

Comparison of the effect of Malva sylvestris L extract ointment and placebo on pain intensity and episiotomy wound healing in primiparous women

Shahid Beheshti University of Medical Sciences0 个研究点目标入组 112 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
112

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 35 years(—)
性别
Female

入选标准

  • Married women aged 18 to 35 years primiparous
  • Being Iranian
  • Gestational age between 37 to 42 weeks
  • No smoking, alcohol and drugs
  • Being literate in reading and writing
  • Having a single fetus with cephalic presentation
  • Fetal weight between 2500 and 4000 gr
  • Body Mass Index (BMI) between 18.5 and 25
  • Vaginal delivery with mediolateral episiotomy
  • The normality of the first, second and third stages of labor

排除标准

  • Amniotic sac rupture more than 24 hours
  • Allergy to Malva sylvestris L ointment
  • Having fever, puerperal infection and hematoma
  • Infant hospitalization at Neonatal Intensive Care Unit
  • Having postpartum hemorrhoids or fissures
  • Having sex in the first ten days after delivery

研究者

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