SLCTR/2021/022已完成4 期
Oral misoprostol Vs intravaginal PGE2 (Dinoprostone) for pre-induction cervical ripening in women with uncomplicated, singleton, post dated pregnancies: a randomized controlled study
适应症
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- one
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
- •Nulliparous pregnant women
- •In a singleton pregnancy
- •At 40 weeks and 5 days of gestation
- •Fetus in cephalic presentation with intact membranes
- •Modified bishop score(MBS) of < 5
- •Not having any contraindications for vaginal delivery
排除标准
- •past caesarian delivery
- •history of myomectomy
- •hypersensitivity to misoprostol
- •pregnancy induced hypertension
- •gestational diabetes mellitus
- •multiple pregnancies
研究者
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