跳至主要内容
临床试验/CTRI/2020/06/025870
CTRI/2020/06/025870尚未招募未知

â?? OPTIMAL CONCENTRATION OF LEVOBUPIVACAINE IN LABOUR PAIN MANAGEMENT USING PARTURIENT CONTROLLED EPIDURAL ANALGESIA (PCEA)â?? a Double-blind, Randomized trial

Dr S N Medical College0 个研究点目标入组 33 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
尚未招募
发起方
入组人数
33

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) American Society of Anesthesiologists (ASA) grade I and II
  • 2) Age >18 years
  • 3) Primigravida
  • 4) Single gestation
  • 5) Cephalic presentation at > 37 wk of gestation
  • 6)In early spontaneous labour (cervical dilation 50% effacement
  • 7) Requesting epidural analgesia for labour

排除标准

  • 1)Refusal by parturient.
  • 2) Systemic and local sepsis.
  • 3)Deranged coagulation profile.
  • 4)Parturients having multiple pregnancies and premature labour.
  • 5)Obstetric complications (e.g., premature rupture of amniotic membranes).
  • 6)Allergy to study drugs, i.e. levobupivacaine and fentanyl.
  • 7)Body mass index >35mg/m2

研究者

发起方
Dr S N Medical College

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