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临床试验/CTRI/2017/08/009542
CTRI/2017/08/009542招募中4 期

To evaluate and compare epidural minimum local analgesic concentration of levobupivacaine with fentanyl in patients receiving intrathecal fentanyl with and without levobupivacaine for labour analgesia - NA

Dr L H Hiranandani Hospital0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
4 期
状态
招募中

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.Primigravida women requesting labour analgesia with full term gestation 36-40 weeks, singleton pregnancy with cephalic presentation having American Society Of Anesthesiologists physical status II
  • 2.Patients giving valid informed consent.
  • 3.Patients in active stage of induced labour with cervical dilatation of 4-5 cm at the time of epidural catheter placement

排除标准

  • 1.Patient refusal
  • 2.Gestational age >36 weeks with malpresentation/ multiple gestation.
  • 3.Patients with PIH / Eclampsia.
  • 4.Patients who have received IV/ IM opioids within 4 hours of epidural insertion.
  • 5.Entered in second stage of labour.
  • 6.Delivery within 30mins of intrathecal analgesia.
  • 7.Delivery without the requirement of epidural top up.
  • 8.Failure to obtain VAS <2 after 15minutes of intrathecal drug injection.
  • 9.Patient with motor block higher than T4 dermatomal level at any time post procedure suspecting intrathecal epidural catheter insertion.
  • 10.Inadvertent dural puncture during epidural space localization.
  • 11. Patients with contraindication to regional analgesia

研究者

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