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临床试验/CTRI/2015/04/005711
CTRI/2015/04/005711已完成未知

Comparison of oral and vaginal misoprostol in induction of labour at term pregnancy in nulliparous women.

Safdarjung Hospital0 个研究点目标入组 200 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
入组人数
200

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

  • Only primiparous women with a live singleton pregnancy, period of gestation >37 weeks with obstetric or medical indications for induction, unfavourable cervix (Bishop score <= 6), cephalic presentation, reactive foetal heart rate pattern and intact membranes.

排除标准

  • Previous uterine incision, allergy to prostaglandin administration, uterine contractions >= 3 in 10 minutes, maternal cardiac, asthma, renal, or hepatic disease, patients on magnesium sulphate therapy, patients with fetal growth restriction, oligohydramnios, leaking or bleeding per vaginum.

研究者

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