SLCTR/2016/024已完成3 期
Oral misoprostol for 48 hours versus an intracervical Foley catheter for 48 hours for induction of labour in post dated pregnancies : a randomized control trial
Department of Obstetrics and Gynecology Faculty of Medicine, University of Ruhuna0 个研究点开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
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
入选标准
- •1. Women with uncomplicated pregnancies
- •2. 40 weeks + 5 days gestation
- •3. Modified Bishop score (MBS) of < 6
- •4. Singleton pregnancy
- •5. Cephalic presentation
- •6. Intact membranes
排除标准
- •1. Pregnancy induced hypertension
- •2. Gestational diabetes mellitus
- •3. Fetal growth restriction
- •4. Previous caesarean delivery
- •5. Scarred uterus
- •6. Hypersensitivity to misoprostol
- •7. Contraindication for a vaginal delivery
研究者
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