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临床试验/IRCT201510118611N1
IRCT201510118611N1已完成1 期

The comparison of the effectiveness of phenytoin cream with placebo on episiotomy healing in primipara women

Vice-Chancellor for Research of Qazvin University of Medical Sciences0 个研究点目标入组 130 人开始时间: 待定最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
130

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

  • The women with 18-35 years old and full term pregnancy (37 to 42 weeks) being nulliparous; no specific diseases (cardiovascular; hepatic; renal; diabetes; coagulopathy diseases; anemia); non- obese (BMI<29; according to the same scale); singelton; cephalic presentation; episiotomy on gynecological bed; time of repair less than 30 minutes; episiotomy repair by chromic catgut sutures. exclusion criteria: Hematomas during and after the repair of episiotomy; extended Episiotomy; excessive bleeding after childbirth; manipulation of the perineum, uterus and cervixe; prolonged rupture of amniotic sac more than 18 hour; use of assistive devices (vacum during delivery); no smoking and alcohol.

排除标准

  • 未提供

研究者

发起方
Vice-Chancellor for Research of Qazvin University of Medical Sciences

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