NL-OMON24831已完成不适用
A randomized clinical trial of ultrasound-guided double percutaneaous needling versus high-energy extracorporeal shockwave therapy in th treatment of calcific tendinopathy of the rotator cuff
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- -
- 入组人数
- 100
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
入选标准
- •Clinical signs of subacromial pain of the Symptoms persisting for more than four Unsuccessful conservative therapy within the previous four months (Physiotherapy, radiotherapy, infiltration with local anaesthetics and/or steroids, anti-inflammatory drugs.)
- •Standardised radiographs showing calcific deposits with a diameter of at least 5 mm
- •oMorphological type-I and type-II deposits corresponding to the classification of Gartner and Simons on radiographs: Type I, sharply outlined and densely structured. Type II, sharply outlined and inhomogenous or homogenous with no defined border
排除标准
- •Evidence of full thickness tears of the rotator cuff on physical examination, ultrasound images or MRI
- •Radiological signs of spontaneous resorption of the deposit and type-III deposits according to the classification of Gartner and Simons: Type III, cloudy and transparent in structure
- •Calcific deposits in multiple tendons of the rotator cuff
- •Acute subacromial/subdeltoid bursitis
- •Osteoarthritis of the glenohumeral or acromioclavicular joint
- •Adhesive capsulitis
- •Previous surgery to the shoulder
- •Instability of the shoulder
- •ESWT / barbotage within the last year
- •Reumatoid arthritis
- •Neurological disorders or dysfunction of the upper limb
- •Heart pacemaker, pregnancy, infection, tumour, hypocoagulability
- •Unability to give informed consent
研究者
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