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.
At a Glance
- Age
- 18 – 75
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 30 (estimated)
- Sponsor
- Ankara City Hospital Bilkent · Other
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
Check Your Eligibility
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
Loading…
Loading trial locations…
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