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临床试验/CTRI/2017/02/007963
CTRI/2017/02/007963已完成未知

Efficacy of oral paracetamol for sparing the dosage of levobupivacaine-fentanyl combination in patient-controlled combined spinal-epidural analgesia in labouring parturients

Government Medical College and Hospital0 个研究点目标入组 60 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
60

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)ASA Grade 1 and 2
  • 2)Age more than 18 years
  • 3)Primigravida Single gestation
  • 4)Cephalic presentation at 36 completed weeks of gestation
  • 5)In early spontaneous labour(cervical dilatation < 5cm)
  • 6)Baseline pain score > 30(on a 0-100 VAS)
  • 7)Able to use PCEA pump
  • 8)Requesting epidural analgesia for labour

排除标准

  • 1)Refusal by parturient
  • 2)Parturients who had received parenteral opiods in the last 4 hours
  • 3)Systemic and local sepsis
  • 4)Deranged coagulation profile
  • 5)Parturients having multiple pregnancies and premature labour
  • 6)Obstetrics complications(eg. PROM)
  • Chorioamnionitis
  • 7)Patients with hepatic and renal impairment
  • 8)Unable to swallow oral tablets
  • 9)HELLP syndrome
  • 10)Noncephalic presentations
  • 11)Allgery to study drugs i.e levobupivacaine,fentanyl,paracetamol

研究者

发起方
Government Medical College and Hospital

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