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Clinical Trials/NL-OMON24831
NL-OMON24831
Completed
N/A

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

-0 sites100 target enrollmentTBD

Overview

Phase
N/A
Intervention
Not specified
Conditions
shoulder, rotator cuff, calcific, tendinopathy, treatment, shockwave, ESWT, barbotage, percutaneous needling, minimally invasive, schouder, tendinosis calcarea
Sponsor
-
Enrollment
100
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Sponsor
-

Eligibility Criteria

Inclusion Criteria

  • 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

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
  • Adhesive capsulitis
  • Previous surgery to the shoulder
  • Instability of the shoulder
  • ESWT / barbotage within the last year
  • Reumatoid arthritis

Outcomes

Primary Outcomes

Not specified

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