Patient Pain and Function in Medial Knee Osteoarthritis After Anteromedial vs Anterolateral Intra-Articular Corticosteroid Injection
- NCT ID
- NCT07804446
- Registry status
- Recruiting
- Study type
- Interventional
- Phase
- Not applicable
- Sponsor
- University of Chicago
- Conditions
- Osteoarthitis, Osteoarthritic Knee Pain, Osteoarthritis (OA), Osteoarthritis (OA) of the Knee, Osteoarthritis in the Knee
Overview
ClinicalTrials.gov lists this study as Recruiting.
Official title: Does Injection Site (Anteromedial vs Anterolateral) Affect Pain Relief After Intra-Articular Corticosteroid Injection in Moderate-to-Severe Medial Knee Osteoarthritis?
Enrollment: 140 participants (Estimated).
What is being studied
- Procedure: Anterolateral Injection
- Procedure: Anteromedial Injection
Who may be eligible
- Ages
- 40 Years to no maximum
- Sex
- All
- Healthy volunteers accepted
- No
ClinicalTrials.gov lists the following eligibility criteria.
Study locations
5 study locations are listed.
Recruiting site status is explicitly provided for 5 locations; 5 are listed as Recruiting.
Countries: United States
- Illinois, United States: 5
Sample of listed locations
- Bolingbrook Clinic — Bolingbrook, Illinois, 60440, United States — Recruiting
- Hyde Park Clinic — Chicago, Illinois, 60637, United States — Recruiting
- La Grange Clinic — La Grange, Illinois, 60525, United States — Recruiting
- Orland Park Clinic — Orland Park, Illinois, 60462, United States — Recruiting
- Woodridge Clinic — Woodridge, Illinois, 60517, United States — Recruiting
Study details
- Start date
- August 31, 2026
- Primary completion date
- April 1, 2027
- Completion date
- May 1, 2027
- First posted
- September 4, 2026
- Collaborators
- AdventHealth
Source and update information
- Source
- ClinicalTrials.gov
- NCT ID
- NCT07804446
- Registry last updated
- September 4, 2026
- QualifiedStudies registry data refreshed
- October 5, 2026
- QualifiedStudies record fetched
- October 5, 2026
View NCT07804446 on ClinicalTrials.gov
Trial information can change. Confirm current study details with the study team or the registry.
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