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Search / Trial NCT05478902

Effectiveness of Non-surgical Management in Rotator Cuff Calcific Tendinopathy (THE EFFECT TRIAL)

Launched by UNIVERSITY OF VALENCIA · Jul 26, 2022

Trial Information

Current as of July 01, 2025

Recruiting

Keywords

Exercise Therapy Lavage Rotator Cuff Calcific Tendinopathy Shoulder Calcification Extracorporeal Shockwave Therapy Ultrasound Guided Percutaneous Irrigation Shoulder Pain Shape Up My Shoulders Sums

ClinConnect Summary

The EFFECT trial is a study looking at different ways to treat a condition called rotator cuff calcific tendinopathy, which causes pain and difficulty moving the shoulder due to calcium deposits in the rotator cuff. Researchers want to see how well an exercise therapy program works compared to two other treatments: extracorporeal shockwave therapy (a non-invasive treatment that uses sound waves) and ultrasound-guided irrigation (a method to wash out the calcium), as well as a "wait and see" approach.

To participate in this trial, you need to be between 18 and 80 years old and have a confirmed calcium deposit in your rotator cuff, along with shoulder pain and reduced movement. You should not be currently receiving any physiotherapy or shockwave therapy. If you join the study, you'll be assigned to one of the treatment groups and will be monitored to see how well the treatment helps with your pain and shoulder function. This trial is currently looking for volunteers, so if you're interested, it could be a good opportunity to explore treatment options for your shoulder pain.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • calcification deposit in the rotator cuff confirmed by diagnostic imaging (ultrasound, MRI or X-ray);
  • pain and loss of function in the shoulder;
  • not currently receiving physiotherapy or ESWT.
  • Exclusion Criteria:
  • previous treatments on last year (e.g., injections, ESWT, US-PICT, surgery, etc.);
  • other shoulder disorders or trauma (e.g., fractures, dislocations, rotator cuff tears, frozen shoulder or shoulder instability);
  • known allergy to any of the pharmacological products used in the study;
  • taking oral anticoagulants
  • taking oral steroid within the six months prior to participation in the study;
  • cancer, systemic disease, pregnancy or infection;
  • neck pain.

About University Of Valencia

The University of Valencia, a prestigious institution located in Spain, is dedicated to advancing scientific knowledge and improving public health through innovative research. With a strong emphasis on interdisciplinary collaboration, the university engages in a wide array of clinical trials aimed at addressing pressing medical challenges. Its commitment to ethical standards and regulatory compliance ensures the integrity of its research initiatives, while its experienced team of researchers and clinicians work diligently to translate scientific discoveries into practical applications that benefit patients and communities. The University of Valencia is at the forefront of medical research, fostering a culture of excellence and innovation in the pursuit of better healthcare solutions.

Locations

Valencia, , Spain

Xativa, Valencia, Spain

Patients applied

0 patients applied

Trial Officials

Enrique Lluch, PT, PhD

Study Director

University of Valencia

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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