IRCT20200316046795N1尚未招募3 期
Effect of oral evening primrose capsules on ripening of the cervix and progress of delivery in primiparous women
Sanandaj University of Medical Sciences0 个研究点目标入组 112 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 112
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
- •Willingness to participate in the study
- •Being primiparous
- •Literacy for reading and writing
- •Age 18 to 35 years old
- •Term pregnancy age (gestational age 39 weeks to 39 weeks and 6 days) based on first trimester ultrasound
- •Single-pregnancy whit cephalic presentation
- •Having a normal pelvis with a gynecologist's diagnosis
- •The estimated weight of the fetus is between 4000-2500 grams
- •Bishop score lower than or equal to 4
- •Intact membranes
- •Healthy pregnant women (without known disease, surgery or pregnancy complications such as placental abruption, placenta previa or vasoprevia , preeclampsia or no fetal anomaly)
- •No ban on the use of evening primrose oil (hemorrhagic disorders, consuming anticoagulants, individuals with a history of schizophrenia, epilepsy and consumer phenothiazine)
- •No structural cervical anomalies
- •Height above 150 cm
- •Lack of alcohol and opioids
- •Avoid using laxatives and any herbal medication prior to study
排除标准
- •Mother's unwillingness to continue cooperation in the research
- •Consumption of less than two capsules per day (problems with checklist of oral capsules)
- •Use of epidural anesthesia
- •Cesarean delivery
研究者
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