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临床试验/NCT01018277
NCT01018277已完成不适用

Effect of Mobilization on Acute Postoperative Pain and Nociceptive Function After Total Knee Arthroplasty: A Prospective, Consecutive, Trial

Hvidovre University Hospital1 个研究点 分布在 1 个国家目标入组 26 人开始时间: 2009年12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
26
试验地点
1
主要终点
Pain score on the visual analog scale (difference before and after two mobilisation seances)

研究概览

简要总结

Aim of the present study is twofold.

  • First we want to evaluate the effect of mobilization on acute postoperative pain
  • Second to test weather chances in pain sensitivity are occurring following surgery and mobilization after total knee arthroplasty

详细描述

Little is known about the effect of mobilization on acute postoperative pain and mobilization induced pain, and if altered pain sensitivity occur under these circumstances.

  • First we want to evaluate the effect of mobilization on acute postoperative pain using the visual analog scale (VAS)
  • Second to test weather chances in pain sensitivity are occurring following surgery and mobilization after total knee arthroplasty, using two simple tools, the Pain Matcher and a Pressure Algometer.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients scheduled for total unilateral knee arthroplasty

排除标准

  • Cognitive dysfunction or peripheral / central neurological dysfunction inconsistent with protocol completing
  • Alcohol and medical abuse (as defined by the National Health Service of Denmark
  • Daily use of opioids or glucocorticoids

结局指标

主要结局

Pain score on the visual analog scale (difference before and after two mobilisation seances)

时间窗: up to 24 hours

pain at rest (supine) 5 min after exercise(after the 2nd walk)

次要结局

  • Pain score on the visual analog scale (difference before and after two mobilisation seances)(up to 24 hours)
  • Pain sensitivity measured with pressure algometry and with pain matcher (difference before and after two mobilisation seances and difference before and after surgery)(up to 24 hours)

研究者

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

Troels Haxholdt Lunn

MD

Hvidovre University Hospital

研究点 (1)

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