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临床试验/IRCT20201028049169N1
IRCT20201028049169N1招募中3 期

Comparison of the effect of Evening primrose oil with vaginal misoprostol in softening of the cervix in patients candidate for myomectomy hysteroscopy in Yas Hospital 2020-2022: a Randomized Clinical Trial

Tehran University of Medical Sciences0 个研究点目标入组 118 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
招募中
入组人数
118

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
25 years 至 75 years(—)
性别
Female

入选标准

  • All non-menopausal nulliparous women or Gravid One women with a history of one cesarean section
  • The age group of 25 to 75 years

排除标准

  • people with a history of schizophrenia or epilepsy taking phenothiazines, structural cervical abnormalities such as a history of cervical insufficiency, Müllerian anomaly, and history of conization
  • The unwillingness of people to participate in the study
  • Allergy to Evening primrose oil or misoprostol
  • contraindications for Evening primrose oil or misoprostol using such as coagulation disorders or concomitant consumption of anticoagulants drug

研究者

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