跳至主要内容
临床试验/NL-OMON47590
NL-OMON47590撤回不适用

Central pain sensitisation or (peri)articular damage: the origin of pain in SAPS A randomised, placebo controlled, blinded, cross-over trial - PARTItrial

eids Universitair Medisch Centrum0 个研究点目标入组 40 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
入组人数
40

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

年龄范围
18 至 99(—)

入选标准

  • - Chronic shoulder pain (>3 months)
  • - Unilateral shoulder pain
  • - Suspicion of subacromial origin of pain (e.g. positive painful arc test, Hawkins-Kennedy test, empty can test)
  • - Presence of conventional ultrasonography
  • - Presence of conventional radiographs

排除标准

  • - Younger than 18 years of age
  • - Tendinitis calcarea
  • - Full thickness rotator cuff tear
  • - Suspicion of capsulitis adhesiva after clinical examination
  • - Glenohumeral osteoarthritis
  • - Medication that potentially act on central pain sensitisation (e.g. pregabalin, amitriptylin, duloxetine)
  • - Use of opioid analgesics, e.g. oxycodone.
  • - Suspicion of symptomatic acromioclavicular osteoarthritis (e.g. positive cross body adduction test)
  • - History of fractures or dislocations of the shoulder
  • - Cardiac disease
  • - Comorbidities: neurological disorders (e.g. plexus lesion), rheumatic disorders (e.g. polymyalgia rheumatic), muscle dystrophies, metabolic disorders (e.g. hypothyreodism), neoplasms
  • - Diagnosed with other chronic pain syndrome, e.g. diabetic polyneuropathy, chronic low back pain or fibromyalgia
  • - Insufficient Dutch language skills
  • - No informed consent

研究者

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