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临床试验/IRCT20210113050028N2
IRCT20210113050028N2招募中3 期

Comparison of the effect of vaginal misoprostol alone and in combination with Evening primrose Capsule on the state of delivery in pregnant women candidate for pregnancy termination

Ardabil University of Medical Sciences0 个研究点目标入组 30 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
招募中
入组人数
30

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
15 years 至 45 years(—)
性别
Female

入选标准

  • Single pregnancy
  • Fetal weight less than 4 kg
  • Amniotic fluid index more than 5 cm
  • normal fetus NST
  • Bishop score less than 7
  • Absence of labor pains in the mother

排除标准

  • Rupture of membranes
  • Possibility of fetal abnormalities
  • need for urgent delivery
  • Hypersensitivity to prostaglandins and evening primrose
  • History of seizures
  • history of schizophrenia with phenothiazin Prescription
  • Bleeding disorders or taking anticoagulants
  • Fallen in FHR
  • Malpresentation
  • Fetal disorders such as hydrocephalia

研究者

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