NL-OMON40188
Recruiting
N/A
A randomized clinical trial of ultrasound-guided double percutaneous needling versus high-energy extracorporeal shockwave therapy in the treatment of calcific tendinopathy of the rotator cuff. - nvt
Spaarne Ziekenhuis0 sites100 target enrollmentTBD
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- calcific tendinopathy
- Sponsor
- Spaarne Ziekenhuis
- Enrollment
- 100
- Status
- Recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Age \> 18 years
- •Clinical signs of subacromial impingement of the shoulder
- •Symptoms persisting for more than four months
- •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. (Morphological 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)
Exclusion Criteria
- •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.
- •Previous surgery to the shoulder.
- •Adhesive capsulitis
- •Instability of the shoulder.
- •ESWT / barbotage within the last year.
- •Reumatoid arthritis.
Outcomes
Primary Outcomes
Not specified
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