Actively Recruiting
A Randomized Comparative Cohort Study of Intra-articular Corticosteroid Injection Versus Suprascapular Nerve Block for Shoulder Pain Treatment
Led by University of Minnesota · Updated on 2026-01-08
40
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating two types of conservative pain relief methods for patients with glenohumeral arthritis or rotator cuff arthropathy who are poor candidates for surgery or prefer not to undergo surgery. The study compares intraarticular corticosteroid injections and suprascapular nerve blocks as options for managing shoulder pain in this population. This randomized, double-masked study is sponsored by the University of Minnesota and aims to understand which treatment better helps reduce pain and improve shoulder function. Participants are randomly assigned to receive either an intraarticular corticosteroid injection or a suprascapular nerve block. The corticosteroid injection involves ultrasound-guided injection of methylprednisolone acetate directly into the shoulder joint. The suprascapular nerve block uses ultrasound guidance to inject a mixture of bupivacaine and triamcinolone near the suprascapular nerve to block pain signals. Both procedures are performed while the patient is seated and use ultrasound for precise delivery. During the study, participants will have their pain and shoulder function assessed before treatment and at multiple time points after intervention: 24 hours, 3 days, 1 month, and 3 months. Measurements include the visual analog scale for pain, single assessment numerical evaluation, Oxford shoulder score, and American shoulder and elbow surgeons score. These assessments help researchers compare the effects of the two treatments over time. The total study participation period extends up to 3 months post-intervention for each patient.
CONDITIONS
Brief Title
Corticosteroid Injection Versus Nerve Block
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of glenohumeral osteoarthritis, rheumatoid arthritis, or rotator cuff arthropathy
- Being offered injection treatment
- Age between 18 and 99 years
You will not qualify if you...
- Uncontrolled diabetes (no HbA1c within a year or HbA1c of 8 or greater)
- Known allergy to steroids or anesthetics
- Pregnant women
- Prisoners
- Patients unable to consent to participation
- Children under 18 years
- Non-English speakers
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Single treatment visit
Participants receive either an intraarticular corticosteroid injection or a suprascapular nerve block to treat shoulder pain.
1 treatment visit (in-person)
Duration - 3 months
Participants are assessed for pain and shoulder function at multiple time points after treatment to monitor effectiveness.
Visits at 24 hours, 3 days, 1 month, and 3 months post-treatment
Trial Site Locations
Total: 1 location
1
University of Minnesota
Minneapolis, Minnesota, United States, 55414
Actively Recruiting
Research Team
A
Allison Rao
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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