PACTR202407560838827尚未招募3 期
Cervical ripening /Labour induction in postdate nulliparas; Comparative study of vaginal misoprostol versus vaginal misoprostol with rectal hyoscine-butylbromide
未提供0 个研究点目标入组 70 人开始时间: 2024年6月29日最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 入组人数
- 70
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
- •1. Those who will give consent to the study.
- •2. Nulliparous pregnant women.
- •3. Postdate pregnancy.
- •4. Selected for cervical ripening and induction of labour.
- •5 Singleton pregnancy with vertex presentation.
排除标准
- •1. maternal co-morbidities like hypertension, diabetes Mellitus,
- •2. Pregnancy complications like antepartum haemorrhage and severe pre-eclampsia
- •Those allergic to hyoscine
- •Those contraindicated to receive prostaglandins like asthma and glaucoma
- •5. Previous caesarian scar
- •6. Contraindication to vaginal delivery
- •Malpresentation
研究者
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