跳至主要内容
临床试验/CTRI/2018/09/015751
CTRI/2018/09/015751已完成未知

Intravenous dexamethasone as an adjunct to epidural labour analgesia with 0.125% ropivacaine in parturients.

A0 个研究点目标入组 80 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
发起方
A
入组人数
80

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.Parturients in established labour with cervical dilation >3cm, with intact or absent membranes and having satisfactory uterine contractions with >50% effacement.
  • 2.Singleton pregnancy with vertex presentation at term,
  • 3.Primigravidaor gravida 2 (previously normal delivered),
  • 4.Age 18 years or above, weight less than 100kg, height 150 cm or more.

排除标准

  • 1.Patient refusal,
  • 2.Any fetal anomalies,
  • 3.History of coagulation disorders,
  • 4.Any contraindications to epidural anaesthesia,
  • 5.History of allergy to local anaesthetics,
  • 6.Any obstetric complications (e.g., premature rupture of amniotic membranes,PIH),
  • 7.Systemic and local sepsis,
  • 8.Parturients having multiple pregnancies and premature labour,
  • 9.History of peptic ulcer disease,
  • 10.Known case of uncontrolled diabetes mellitus, and patient who had received dexamethasone in last 7 days for fetal lung maturity.

研究者

发起方
A

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