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临床试验/NCT00637013
NCT00637013进行中(未招募)不适用

The Effectiveness and Cost-effectiveness of Operative Versus Non-operative Management of Subacromial Impingement

Central Finland Hospital District4 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2008年6月1日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
100
试验地点
4
主要终点
Change in pain (VAS) and objective shoulder function (Constant score)

研究概览

简要总结

The study aims at determining the effectiveness and cost-effectiveness of surgical management of subacromial impingement (including partial tears) compared to conservative treatment. The research setting is prospective, randomised, and controlled.

The aim of the study is to search out evidence based data of indications for subacromial decompression. The investigators also aim at offering patients the most efficient and effective treatment and reduce the number of operations that do not have sufficient effectiveness. The data obtained will facilitate developing guidelines for referrals to a specialist when subacromial impingement is suspected.

The investigators hypothesise that there are subgroups of patients suffering from subacromial impingement that benefit from surgery whereas other subgroups are best treated conservatively.

详细描述

Subgroup analysis:

  • age
  • sex
  • duration of symptoms
  • presence of trauma before symptoms
  • presence of partial tear
  • degenerative findings
  • other findings in MRI or arthroscopy
  • type of operation
  • co-morbidities
  • occupation
  • pain (VAS)
  • objective shoulder function
  • activities of daily living

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
None

入排标准

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

入选标准

  • age over 35 years old
  • duration of symptoms at least three months despite non-operative treatment
  • accepts both treatment options (operative and physical therapy)
  • must have pain in abduction of the shoulder
  • must have painful arc
  • must have pain in two of the three isometric tests (0 and 30 degrees of abduction, or external rotation)
  • a positive result in the impingement test (a subacromial injection of lidocaine reduces pain)

排除标准

  • previous shoulder operations
  • too high risk for operation
  • any disease or social problem reducing the ability to co-operate
  • rheumatoid arthritis
  • severe arthrosis of the glenohumeral or acromioclavicular joint
  • a full-thickness rotator cuff tear in MRI arthrography
  • a progressive malign disease
  • adhesive capsulitis
  • high-energy trauma before symptoms
  • cervical syndrome
  • shoulder instability

结局指标

主要结局

Change in pain (VAS) and objective shoulder function (Constant score)

时间窗: 24 months after intervention

VAS (0 to 100 mm), Constant score (0 to 100 points)

次要结局

  • Change in pain (VAS) and objective shoulder function (Constant score)(5 years after uintervention)

研究者

发起方
Central Finland Hospital District
申办方类型
Other
责任方
Principal Investigator
主要研究者

Juha Paloneva

Md, PhD

Central Finland Hospital District

研究点 (4)

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