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临床试验/CTRI/2017/03/008018
CTRI/2017/03/008018已完成4 期

Efficacy of transdermal buprenorphine patch on postoperative pain relief after elective spinal instrumentation surgery

Bangur Institute of Neurology0 个研究点目标入组 70 人开始时间: 待定最近更新:

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
70

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

  • ASA I or ASA II
  • Age between 20-50 yrs
  • Weight between (50-65kg)
  • Patients of either sex.
  • Patients scheduled for elective spinal instrumentation surgery
  • Anticipated duration of surgery 2-3 hrs.

排除标准

  • Patient refusal
  • Neurological disorders and history of seizure
  • Patient on CNS depressant drug
  • Known allergic to opioids
  • Opioid dependent patient
  • Hemodynamically compromised patients
  • Patient with hepatic impairment

研究者

发起方
Bangur Institute of Neurology

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