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临床试验/IRCT20220315054298N1
IRCT20220315054298N1尚未招募2 期

comparison of the Effectiveness of pre-operative intravenous ketamine administration with placebo in controlling post-operative pain in patients with advanced knee osteoarthritis undergoing total knee arthroplasty

Tehran University of Medical Sciences0 个研究点目标入组 60 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
尚未招募
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

入排标准

年龄范围
18 years 至 85 years(—)
性别
All

入选标准

  • Between 18 and 85 years old
  • undergoing unilateral, primary total knee arthroplasty TKA for degenerative end-stage osteoarthritis(OA) of the knee (score of >2 on Kellgren-Lawrence scale).

排除标准

  • patients who refuse to participate,
  • classified as ASA IV or V by the American Society of Anesthesiologists,
  • body mass index greater than 40 kg/m2,
  • rheumatoid arthritis,
  • contraindication or allergy to opioid pain medications
  • allergy to amide or sulpha anesthetics,
  • unable to understand the visual analog scale (VAS) ,
  • any preoperative ketamine or chronic narcotic usage (>10mg systemic morphine equivalents daily ) as it causes opioids tolerance ,
  • those who are discharged before the first 24 hours postoperatively,
  • previous history of knee arthroplasty,
  • prior surgery on the ipsilateral knee within 6 months,
  • simultaneous bilateral arthroplasty,
  • the patients receiving general anesthesia or a nerve block
  • patients with an ejection fraction of less than 30%,
  • creatinine clearance of less than 30mL/min,
  • chronic liver disease,
  • any neurologic or psychiatric disorder (including bipolar,post-traumatic stress disorder, schizophrenia),
  • chronic alcohol abuse

研究者

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