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临床试验/TCTR20201228004
TCTR20201228004尚未招募未知

Multimodal analgesia study of nefopam combined with ketorolac, paracetamol and gabapentin compare to morphine in postoperative unilateral total knee arthroplasty

erdsin hospital0 个研究点目标入组 100 人开始时间: 2020年12月28日最近更新:
适应症

试验速览

阶段
未知
状态
尚未招募
发起方
入组人数
100

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
0 N/A (No limit) 至 0 N/A (No limit)(—)
性别
All

入选标准

  • 1.Postoperative unilateral total knee arthroplasty patients.
  • 2.Patients whose medial collateral ligament were not released
  • 3.Underwent spinal block without morphine injection to subarachnoid space

排除标准

  • 1.Cannot give information about VAS
  • 2.History of knee surgery same side of total knee arthroplasty
  • 3.BMI equal or more than 40 kg/square meters
  • 4.Underlying disease that are contraindicated to nefopam, ketorolac, paracetamol, gabapentin, morphine : chronic liver disease, cardiac or chronic renal failure(GFR < 90 ml/min/1.73m2), psychiatric disorder, alcohol abuse, glaucoma, peptic ulcer, inflammatory bowel disease, established, ischemic heart disease, suicidal idea
  • 5.History of drug allergy to sulfonamides group
  • 6.Allergy to aspirin, NSAIDs, selective COX-2 inhibitors

研究者

发起方
erdsin hospital

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