跳至主要内容
临床试验/CTRI/2023/02/049668
CTRI/2023/02/049668进行中(未招募)4 期

Comparison of interleukins in parturients with combined spinal epidural versus epidural undergoing labour analgesia

Department of Anaesthesia and Intensive Care0 个研究点目标入组 40 人开始时间: 待定最近更新:

试验速览

阶段
4 期
状态
进行中(未招募)
发起方
入组人数
40

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 Anaesthesiologists (ASA) grade I and II
  • 2.Age >18 years
  • 3.Primigravida
  • 4.Single gestation
  • 5.Cephalic presentation at = 36 weeks of gestation
  • 6.In true labour (cervical dilation = 5 cm)
  • 7.Baseline pain score > 30 (on a 0-100 VAS)
  • 8.Able to use PCEA pump
  • 9.Requesting epidural analgesia for labour

排除标准

  • 1.Refusal by parturient
  • 2.Obesity (weight >100kg)
  • 3.Parturient who had received parenteral opioids in the last 4 hours
  • 4.Systemic and local sepsis
  • 5.Deranged coagulation profile
  • 6.Parturients having multiple pregnancies
  • 7.Obstetric complications (e.g., premature rupture of amniotic membranes, premature labour, eclampsia, antepartum hemorrhage, chorioamionitis, HELLP syndrome)
  • 8.Noncephalic presentations
  • 9.Allergy to study drugs, i.e., levobupivacaine, fentanyl.
  • 10.Patient with history of immunosuppresion

研究者

发起方
Department of Anaesthesia and Intensive Care

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