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临床试验/IRCT20100303003485N5
IRCT20100303003485N5已完成3 期

The effect of sildenafil citrate on fetal distress during labor and cesarean section - a double-blind clinical trial with placebo

Rasht University of Medical Sciences0 个研究点目标入组 104 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
104

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 between 18-40 years
  • Single pregnancy
  • Term pregnancy (37-41 weeks)
  • Normal fetal structure and without any anomalies
  • Cephalic presentation
  • Estimated weight above 2500 grams
  • Without CPD
  • Candidate for normal vaginal delivery

排除标准

  • Drug reaction to Sildenafil
  • Fetal anomalies
  • Metabolic disorder
  • Cardiac disorders
  • Renal disorders
  • Visual disorders
  • Liver anomalies
  • Previous cesarean
  • Preeclampsia
  • Taking medications Nitrate

研究者

发起方
Rasht University of Medical Sciences

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