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临床试验/IRCT20091023002624N26
IRCT20091023002624N26已完成2 期

A comparative study on the efficacy of nifedipine and indomethacin for prevention of preterm birth as monotherapy and combination therapy

Iran University of Medical Sciences0 个研究点目标入组 150 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
已完成
入组人数
150

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

  • gestational age of 26 to 34 weeks
  • uterine contractions with a frequency of at least 4 forceful uterine contractions per 20 minutes or a cervical dilatation of minimum 1 cm and minimum 50% cervical effacement.

排除标准

  • rupture of membrane
  • intrauterine fetal death
  • cervical dilatation of more than 5 cm
  • multiple pregnancy
  • receiving tocolytic within past 24 hours
  • polyhydramnios
  • preeclampsia and eclampsia
  • vaginal bleeding more than bloody show
  • any maternal and fetal condition that contradict with receiving tocolitics
  • severe fetal anomalies contradict fetal life
  • fetal distress

研究者

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