Novel Treatment for Rotator Cuff Tears
Recruiting now · Not applicable
Conditions studied: Supraspinatus Tear
In brief
The focus of this study is to examine changes in pain scores, strength, and range of motion over time following an ultrasonic tenotomy on a partial tear (\<50%) of the supraspinatus tendon of the rotator cuff.
Key facts
- Study ID
- NCT05590494
- Run by
- Mayo Clinic
- People needed
- 15
- Starts
- 2022-11-07
- Expected to finish
- 2028-12-01
- Last updated by the study team
- 2026-08-05
Who can join
Age: 25 and older, up to 75. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Evidence of partial tear (< 50%) of the supraspinatus tendon on MRI.
You may not qualify if…
- A tear of the supraspinatus tendon greater > 50% and any areas of full thickness tearing, concomitant tears > 25% of other rotator cuff tendons (infraspinatus, teres minor or subscapularis), or acute tear of the glenoid labrum.
- Evidence of systemic illness/infection requiring oral or IV antibiotics during the recruitment period.
- Evidence of overlying skin infection or lesion at the proposed device insertion point on the shoulder.
- Previous corticosteroid injection within three months.
- Those individuals less than 25 and greater than 75 years of age will be excluded.
Where it is running
- Mayo Clinic Health System - Onalaska — Onalaska, Wisconsin, United States (enrolling)
Full record on ClinicalTrials.gov
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