ISRCTN51511455已完成未知
Hyaluronic acid versus corticosteroids compared to a placebo in subacromial injections for shoulder cuff inpingement
Care and Public Health Research Institute (CAPHRI) (The Netherlands)0 个研究点目标入组 159 人开始时间: 2005年12月20日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 159
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
- 性别
- All
入选标准
- •1. Patients 18 years of age and older
- •2. Consult a physician for pain in the shoulder either at rest or elicited or provoked during movement of the shoulder
- •3. Must have a painful arc, with or without a disturbed scapulohumeral movement. The diagnosis is subacromial impingement syndrome.
排除标准
- •1. Pain lasting less than 6 weeks
- •2. Prior injection with corticosteroids last 3 months, less than 100 degrees range of ante-flexion
- •3. More than 50% restriction of external glenohumeral rotation (compared to the non-affected side)
- •4. Steroid or lidocaine allergy
- •5. Pregnancy or supposed pregnancy
- •6. Dementia
- •7. (Prior) purulent infection of the shoulder joints
- •8. Tumour, osteoporosis, rheumatoid arthritis (American College of Rheumatology [ACR] criteria), referred pain from internal organs, or a cervical radicular syndrome as suspected or definite cause for SD
- •9. Stroke, polyneuropathy, multiple sclerosis, polymyalgia, ankylosing spondylitis (modified NY criteria) as suspected or definite cause for SD
- •10. Whiplash, prior fractures or surgery of the shoulder, upper limb, neck or thorax
- •11. Currently receiving (or needing) treatment for serious behavioral, cognitive or psychiatric disorders
- •12. Not able to complete Dutch questionnaires independently and those who are reluctant to adhere to (allocated) treatments or to complete follow-up will be excluded
研究者
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