Intralesional Versus Perilesional 5% Dextrose Injection in Partial Rotator Cuff Tears

Recruiting N/A Interventional Study
Partial Rotator Cuff Tears Rotator Cuff Tendinopathy Shoulder Pain Chronic Supraspinatus Tendon Tear
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 – 75
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
30 (estimated)
Sponsor
Ankara City Hospital Bilkent · Other
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About This Trial
This prospective, randomized, double-blind controlled clinical trial aims to compare the clinical and ultrasonographic outcomes of intralesional and perilesional 5% dextrose injection in patients with partial rotator cuff tears. Eligible participants will be randomized into two parallel groups. Both groups will receive ultrasound-guided 5% dextrose injection to the supraspinatus enthesis. In addit…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Diagnosis of partial rotator cuff tear by a specialist physician after appropriate clinical examination and imaging evaluation * Shoulder pain and functional limitation lasting for at least 3 months * Clinically confirmed shoulder impingement findings, defined as at least one …
Contacts

Esra Ülgen Kıratlıoğlu, MD

+905079614194

esraulgen@gmail.com

CONTACT