跳至主要内容
临床试验/IRCT20210829052319N1
IRCT20210829052319N1尚未招募3 期

Comparison of the postoperative epidural analgesic efficacy between epidural catheter and surgical hemo-vac drain with epidural injection capability in posterior lumbar surgeries

Karaj University of Medical Sciences0 个研究点目标入组 52 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
尚未招募
发起方
入组人数
52

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

年龄范围
18 years 至 65 years(—)
性别
All

入选标准

  • written consent to participate in the study
  • age 18 to 65
  • candidate for instrumentation in posterior lumbar spine surgeries
  • ASA class I-II

排除标准

  • patients withholding consent
  • fracture in the area of surgery
  • speech impairments
  • mental retardation
  • preoperative neurological disorders
  • allergy to anesthetic drugs
  • patients with pacemaker
  • patients that have used ropivacaine, opioids, and NSAIDs one week before the surgery
  • failure in epidural catheter placement during the surgery
  • nausea and vomiting
  • severe hemodynamic changes such as bradycardia or blood pressure drop higher than 30% of average blood pressure
  • severe headache
  • progressive paresthesia of the lower limbs
  • decreased level of consciousness
  • changes in respiratory rate and order

研究者

发起方
Karaj University of Medical Sciences

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