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临床试验/NCT01470391
NCT01470391已完成不适用

"A Comparison of the Efficacy of the Adductor-Canal-Blockade Versus the Femoral Nerve Block on Muscle Strength, Pain and Mobilization After Total Knee Arthroplasty: a Randomized Study

Rigshospitalet, Denmark2 个研究点 分布在 1 个国家目标入组 54 人开始时间: 2011年11月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
54
试验地点
2
主要终点
The difference in quadriceps muscle strength between the Adductor-Canal-Blockade and the femoral nerve block

研究概览

简要总结

The aim of this study is to investigate the efficacy of the Adductor-Canal-Blockade versus the Femoral Nerve Block on muscle strength, pain and mobilization after total knee arthroplasty. We hypothesize that the Adductor-Canal-Blockade has the same effect on pain and morphine consumption as the Femoral Nerve Block, but without the same reduction in quadriceps muscle strength.

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
50 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • BMI > 18 og < 40
  • total knee arthroplasty in spinal anesthesia

排除标准

  • Can not cooperate to the exam
  • Do not speak or understand Danish
  • Drug allergy
  • Alcohol or drug abuse
  • Daily consumption of strong opioids
  • Rheumatoid arthritis
  • Intake of glucocorticoids
  • Effect of spinal anesthesia stopped prior to performing the regional block

结局指标

主要结局

The difference in quadriceps muscle strength between the Adductor-Canal-Blockade and the femoral nerve block

时间窗: 24 h postoperatively

次要结局

  • The difference in adductor muscle strength between the Adductor-Canal-Blockade and the Femoral Nerve Block(24 h postoperatively)
  • Pain during flexion of the knee(2-24 hours)
  • Pain at rest(2-24 hours)
  • Total morphine consumption(0-24 hours)
  • Postoperative nausea(2-24 hours)
  • Postoperative vomiting(0-24 hours)
  • Sedation(2-24 hours)
  • Zofran consumption(0-24 hours)
  • The difference in mobilization between the groups(24 hours)

研究者

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

Pia Jaeger

MD

Rigshospitalet, Denmark

研究点 (2)

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