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临床试验/CTRI/2017/11/010496
CTRI/2017/11/010496已完成4 期

Efficacy of different infusion rates of oxytocin for maintaining uterine tone during non-elective caesarean section in labouring patientsâ?? a randomized, double-blind controlled trial

niversity College of Medical Sciences and GTB Hospital0 个研究点目标入组 105 人开始时间: 待定最近更新:

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
105

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

  • Healthy females with 37 weeks or more gestation,
  • Uncomplicated, singleton pregnancy,
  • Labouring patients who have received oxytocin for induction or augmentation of labour

排除标准

  • Known drug allergy to oxytocin,
  • Maternal complications e.g. pre-eclampsia, diabetes mellitus, cardiovascular disease, cerebrovascular disease, bronchial asthma,
  • Known risk factors for postpartum haemorrhage e.g. Multiple gestation, abnormal placentation, uterine fibroid, macrosomia, hydramnios, history of postpartum haemorrhage or uterine atony

研究者

发起方
niversity College of Medical Sciences and GTB Hospital

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