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临床试验/ACTRN12614000169640
ACTRN12614000169640已完成1 期

Comparison of Analgesia Nociception Index (ANI) guided analgesia administration with Standard Clinical Practice during Routine General Anaesthesia on post-operative pain scores and post-operative opioid requirement in patients undergoing spinal surgery

The University of Adelaide0 个研究点目标入组 60 人开始时间: 2014年2月11日最近更新:

试验速览

阶段
1 期
状态
已完成
入组人数
60

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Open (masking not used)

入排标准

年龄范围
18 Years 至 75 Years(—)
性别
All

入选标准

  • Patients scheduled for non-emergent, spinal surgery, aged 18-75 years, American Society of Anesthesiologists (ASA) score 1 or 2, competent to consent to participation, able to use a Visual Analogue Scale (VAS) and able to activate a patient controlled analgesia (PCA) machine post-operatively.

排除标准

  • Emergency surgery
  • Inability to consent, lack of written consent or speak English fluently
  • Pregnancy or lactation. Pregnancy test will be performed in all women of child bearing potential
  • Cardiac morbidity
  • Non-regular sinus cardiac rhythym
  • Cardiac disease which impacts usual daily functioning (equivalent to ASA greater than or equal to 3)
  • Implanted cardiac pacemaker
  • Concurrent medications with a major effect affect upon the sinus node
  • Expected duration of surgery greater than 3 hours (180 minutes)
  • Extremes of weight (Body Mass Index less than or equal to 19 or greater than or equal to 35 kg per meter squared)
  • Pre-operative chronic opioid use or chronic pain, equivalent to oxycodone 20mg per oral, per day for more than 6 weeks
  • Allergy or intolerance to any of the study drugs
  • Use of neuraxial anaesthesia

研究者

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