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临床试验/NCT01191593
NCT01191593已完成4 期

The Efficacy of Adductor-Canal-Blockade on Pain and Morphine Consumption After Revision Knee Arthroplasty

Rigshospitalet, Denmark2 个研究点 分布在 1 个国家目标入组 36 人开始时间: 2010年9月最近更新:
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适应症

试验速览

阶段
4 期
状态
已完成
入组人数
36
试验地点
2
主要终点
Pain during 45 degrees active flexion of the knee
研究概览研究设计入排标准结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

The purpose of this study is to determine whether Adductor-Canal-Blockade is effective at reducing pain and morphine consumption after revision knee arthroplasty.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
40 Years 至 85 Years（Adult, Older Adult）
性别
All
接受健康志愿者
否

入选标准

  • •Revision Knee Arthroplasty in general anaesthesia
  • •American society of anesthesiologists (ASA) 1-3
  • •BMI 18-40
  • •Written informed consent

排除标准

  • •Can not cooperate to the exam
  • •Do not speak or understand Danish
  • •Drug allergy
  • •Alcohol or drug abuse

结局指标

主要结局

Pain during 45 degrees active flexion of the knee

时间窗: 4 hours postoperative

0-100 mm at a visual analogue scale (VAS), at 4 hours postoperative.

次要结局

  • Pain during 45 degrees active flexion of the knee(24 hours postoperative)
  • Pain during rest(24 hours postoperative)
  • Total morphine consumption(0-24 hours postoperative)
  • Postoperative nausea(24 hours postoperative)
  • Postoperative vomiting(0-24 hours postoperative)
  • Zofran consumption(0-24 hours postoperative)
  • Sedation(24 hours postoperative)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Pia Jaeger

M.D.

Rigshospitalet, Denmark

研究点 (2)

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The Efficacy of Adductor-Canal-Blockade on Pain and... | 临床试验