Condition: Partial Rotator Cuff Tears · Rotator Cuff Tendinopathy · Shoulder Pain Chronic · Sponsor: Ankara City Hospital Bilkent
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 addition, one group will receive intralesional 5% dextrose injection, while the other group will receive perilesional 5% dextrose injection using the peppering technique. Injections will be performed in three treatment sessions at 21-day intervals. All participants will receive a home-based exercise program after completion of the injection treatments. Clinical outcomes will be assessed at baseline, 9 weeks, and 12 weeks after treatment, and ultrasonographic outcomes will be assessed at baseline and 12 weeks.
This description comes directly from the study's public registry record.
Esra Ülgen Kıratlıoğlu, MD · +905079614194 · esraulgen@gmail.com
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| Ankara Bilkent City Hospital, Physical Medicine and Rehabilitation Hospital | Ankara, Turkey (Türkiye) | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07688902