Actively Recruiting

Phase Not Applicable
Age: 18Years - 99Years
All Genders
ID06735027

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

Age: 18Years - 99Years
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

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)

Follow-up

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

Loading map...

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

Similar Trials

Prosthesis Versus Active Exercise Program in Patients With R...

Rotator Cuff Arthropathy

Actively Recruiting

8 locations

Retro-Prospective Postmarket Clinical Study for FX Shoulder ...

Humeral Fracture, Proximal

Actively Recruiting

22 locations

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here