Ultrasound-Guided Shock Wave Therapy for Calcific Tendinitis of the Shoulder

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study uses ultrasound to guide non-invasive shock wave therapy aimed at promoting calcific deposit resorption in the shoulder tendons. Eligible adults with chronic, unilateral calcific tendinitis and moderate pain will receive ESWT targeting the calcium deposits. The goal is to determine whether this approach provides meaningful pain relief and improved shoulder function, with safety monitored throughout. The trial relies on imaging to confirm deposit size and location, and employs standard clinical assessments to track outcomes over time.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Age between 20 and 70 years
* Unilateral calcific tendinitis of the shoulder confirmed by clinical physical examination, including a positive Neer's impingement test
* Symptom duration of more than 3 months
* Imaging (radiography and/or high-resolution ultrasound) demonstrating a calcific deposit within a rotator cuff tendon with a maximal diameter greater than 5 mm
* Baseline self-reported pain intensity greater than 4 on the Visual Analog Scale (VAS, 0-10)
* Willing and able to provide written informed consent

Exclusion Criteria:

* Concomitant full-thickness rotator cuff tear
* History of fracture or surgery involving the ipsilateral shoulder
* Coagulopathy, or anticoagulant therapy that cannot be safely discontinued
* Pregnancy or breastfeeding
* Malignancy, particularly involving or adjacent to the shoulder region
* Local infection or skin lesion at the intended treatment site
* Injection therapy to the ipsilateral shoulder within the preceding 6 weeks
* Any other condition that, in the judgment of the investigator, makes the participant unsuitable for participation in the trial

Where it's running

• Wan Fang Hospital, Taipei Medical University
  Taipei, Taipei, Taiwan Recruiting

Study contacts

• Study coordinator: Shih-Wei Huang, MD
• Email: shihwei@tmu.edu.tw
• Phone: +886970747556

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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• Comparing hyaluronic acid and corticosteroid injections for shoulder tendinitis

  This study is testing whether adding hyaluronic acid injections to corticosteroid injections can help people with shoulder tendinitis feel less pain compared to just using corticosteroids alone.

  Recruiting at 2 sites Phase 3 Centre Hospitalier Departemental Vendee · La Roche-sur-Yon and 1 other locations · NCT06376981

How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.