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临床试验/IRCT20201003048910N1
IRCT20201003048910N1已完成3 期

Evaluation of the effect of oral and vaginal isosorbide mononitrate and oral propranolol tablets on cervical preparation before induction in primiparous and term pregnancy

Tehran University of Medical Sciences0 个研究点目标入组 120 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
已完成
入组人数
120

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
21 years 至 30 years(—)
性别
Female

入选标准

  • Includes 37-40 weeks gestation
  • single fetus
  • intact membranes
  • under two bishop scores
  • fetal weight less than 4 kg
  • normal fetal health monitoring result
  • no uterine contractions
  • There were no systemic problems in the history and clinical examination.

排除标准

  • Abnormality of fetal appearance with pelvis or non-cephalic
  • presence of uterine scar
  • previous history of cesarean section
  • history of cervical cone (conization)
  • polyhydramnios
  • history of drug allergy
  • contraindications to vaginal delivery
  • aginal bleeding during third trimester
  • placenta previa
  • multiple pregnancy
  • suspected fetal abnormality
  • bishop score above 3
  • uterine contractions
  • uncertain NST
  • chorioamnionitis
  • history of asthma
  • active genital herpes
  • any contraindications to induction of labor
  • systolic pressure less than 90
  • Cardiovascular disease
  • severe preeclampsia
  • history of headache

研究者

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