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临床试验/IRCT20160308026971N4
IRCT20160308026971N4已完成3 期

Investigation the Effect of vaginal Evening Primrose capsule on cervix preparation in nulliparous Women

Rafsanjan University of Medical Sciences0 个研究点目标入组 86 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
86

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 35 years(—)
性别
Female

入选标准

  • Inclination to participate in the study
  • Tendency to normal delivery
  • Selection of Niknafs hospital for delivery
  • Mother’s age is 18-35 years
  • Gestational age 38 weeks based on first trimester Ultrasonography or reliable IMP
  • Single fetus with cephalic presentation The basis of the results of the last ultrasound
  • Nulliparality
  • the integrity of the embryonic membranes

排除标准

  • Non-use of two successive capsules of Primrose
  • Primrose capsule susceptibility
  • Emergency intervention for maternal or embryonic reasons
  • Unwillingness of the research unit to continue cooperation
  • Vaginal bleeding
  • Presence of contraindications for use of Evening Primrose capsule (diseases associated with disorders Hemorrhagic agents, anticoagulant drugs, Patients with history of psychiatric disorders in the phenothiazine category, and epilepsy patients)
  • History of known chronic disease
  • Pregnancy complications such as Hydromenosis, Oligohydroamenia, Pre-eclampsia, Eclampsia

研究者

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