PACTR202306488956692已完成Unknown
A comparison of the efficacy of concurrent use of intracervical foley catheter balloon and mifepristone to intracervical foley catheter alone for cervical ripening at term: a triple-blind randomized control trial
ESE ADIGBA ONODJOHWOYOVWE0 个研究点目标入组 112 人开始时间: 2023年5月24日最近更新:
适应症
试验速览
- 阶段
- Unknown
- 状态
- 已完成
- 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
- 19 Year(s) 至 44 Year(s)（—）
- 性别
- Female
入选标准
- •All Consented pregnant women with the following:
- •1.Term pregnancy
- •2. Singleton foetus in cephalic presentation
- •3.Intact foetal membrane
- •4.Normal non stress test
- •5.Bishop Score of < 6
- •6.No contraindication to vaginal delivery
- •7.No known allergy or contraindication to Mifepristone.
排除标准
- •1. Preterm pregnancy
- •2. Prolonged pregnancy (=42 weeks gestation)
- •3. Prelabour rupture of foetal membrane
- •4. Previous caesarean section or major uterine surgery
- •5. Bishop score = 6 at admission
- •6. Foetal malpresentation
- •7. Multiple pregnancy
- •8. Intrauterine foetal death,
- •9. Severe intrauterine growth restriction
- •10. Severe oligohydramnios
- •11. Major congenital anomalies
- •12. Allergy or contraindication to use of Mifepristone
- •13. Abnormal or non-reassuring non stress test
- •14. Contraindication to vaginal delivery
研究者
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