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临床试验/CTRI/2014/05/004596
CTRI/2014/05/004596已完成未知

Intravenous dexamethasone as an adjunct to patient-controlled epidural analgesia with levobupivacaine and fentanyl in labour: a randomized, double blind, placebo controlled study - None

GMCH chandigarh0 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
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

  • American Society of Anesthesiologists (ASA) grade I and II
  • Age >18 years
  • Primigravida
  • Single gestation
  • Cephalic presentation at >= 36 wk of gestation
  • In early spontaneous labour (cervical dilation <= 5 cm)
  • Baseline pain score > 30 (on a 0-100 VAS)
  • Able to use PCEA pump
  • Requesting epidural analgesia for labour

排除标准

  • Refusal by parturient.
  • Parturients who had received parenteral opioids in the last 4 hours.
  • Systemic and local sepsis.
  • Deranged coagulation profile.
  • Parturients having multiple pregnancies and premature labour.
  • Obstetric complications (e.g., premature rupture of amniotic membranes).
  • Noncephalic presentations.
  • Allergy to study drugs, i.e. levobupivacaine and fentanyl.
  • H/O peptic ulcer disease.
  • Known case of uncontrolled Diabetes Mellitus.
  • Patient who have received dexamethasone in last 7 days for foetal lung maturity.

研究者

发起方
GMCH chandigarh

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