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Predicting Response to Intra-Articular Corticosteroid Injection in Patients With Osteoarthritis of the Glenohumeral Joint

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University of Florida

Status and phase

Terminated
Phase 4

Conditions

Osteoarthritis of the Glenohumeral Joint

Treatments

Procedure: intraarticular corticosteroid injections (IACSI)
Drug: corticosteroid injections
Device: Ultrasound

Study type

Interventional

Funder types

Other

Identifiers

NCT03232749
IRB201700603-A
OCR18320 (Other Identifier)

Details and patient eligibility

About

This study will examine the effectiveness of a single cortisone injection in patients with shoulder osteoarthritis over a 6-month period, and identify clinical and radiographic factors to help predict how a patient with shoulder osteoarthritis will respond to a cortisone injection utilizing ultrasound guidance.

Full description

The purpose of this study is to assess the effectiveness of intraarticular corticosteroid injections (IACSI) for glenohumeral arthritis by 1) through patient-reported outcomes and 2) identifying clinical and radiographic predictors of IACSI success.

Enrollment

25 patients

Sex

All

Ages

18 to 100 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with a diagnosis of symptomatic primary osteoarthritis of the shoulder will be recruited from the patient population seeking treatment at the Orthopaedics Sports Medicine Institute.
  • those who have failed previous treatment including over-the-counter analgesics and activity modification
  • have elected to receive a medically-indicated, ultrasound-guided IACSI in the shoulder.

Exclusion criteria

  • Patients will be excluded from the study for any of the following reasons:
  • Post traumatic osteoarthritis
  • Inflammatory osteoarthritis
  • Imaging confirmed rotator cuff tear
  • Prior ipsilateral shoulder surgery
  • Memory loss or inability to complete study measures
  • History of allergy to injection medications
  • Diabetic patients with patient-reported fasting blood glucose >200
  • Prior injection in the ipsilateral shoulder within three months

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

25 participants in 1 patient group

symptomatic primary osteoarthritis of the shoulder
Other group
Description:
Subjects enrolled into the study will be those who have failed previous treatment including over-the-counter analgesics and activity modification, and have elected to receive a medically-indicated, ultrasound-guided IACSI in the shoulder
Treatment:
Drug: corticosteroid injections
Device: Ultrasound
Procedure: intraarticular corticosteroid injections (IACSI)

Trial documents
2

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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