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临床试验/IRCT20230416057923N1
IRCT20230416057923N1
尚未招募
2 期

Comparing the efficacy of Pregabalin with Duloxetine in perioperative pain management in knee fractures surgery: A randomized, double-blind, clinical trial

Tehran University of Medical Sciences0 个研究点目标入组 68 人待定

概览

阶段
2 期
干预措施
未指定
疾病 / 适应症
Condition 1: perioperative pain in knee fractures surgery (patella). Condition 2: perioperative pain in knee fractures surgery (upper end of tibia). Condition 3: perioperative pain in knee fractures surgery (lower end of femur).
发起方
Tehran University of Medical Sciences
入组人数
68
状态
尚未招募
最后更新
2年前

概览

简要总结

暂无简介。

注册库
who.int
开始日期
待定
结束日期
待定
最后更新
2年前
研究类型
Interventional
性别
All

研究者

入排标准

入选标准

  • Age 18 to 80 years
  • Patients with fractures around the knee who are hospitalized and undergo surgery
  • The patient is willing to participate in the study and sign the informed consent form.

排除标准

  • History of taking Duloxetine, Pregabalin and Gabapentin within two weeks before surgery
  • History of allergy to study drugs
  • Severe active infection leads to cognitive impairment
  • Severe renal failure (MDRD renal clearance less than 30 ml/min/1\.73m2\)
  • Severe liver failure (Child Pugh C or liver enzymes more than 5 times the maximum normal range)
  • Moderate to severe dependence (according to DSM5 criteria) to opioids or use within 24 hours before entering the study
  • BMI greater than or equal to 40 kg/m2
  • ASA Physical status IV/V
  • Use of epidural anesthesia in surgery
  • Pregnancy and breastfeeding

结局指标

主要结局

未指定

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