ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2025
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • 2020-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings

Abstract Number: 2624

Results of Large Multi-Site Pragmatic Clinical Trial Comparing Corticosteroids or Blinded Lidocaine-only Injections in Treating Osteoarthritis of the Knee

Joshua Baker1, Katherine Wysham2, Mercedes Quinones3, Bryant England4, Kaitian Jin1, Marianna Olave5, Sarah Wetzel6, Rachel Gillcrist7, Criswell Lavery1, Natalie Keller8, Kimberly Hayes9, Bridget Kramer4, Hannah Brubeck10, Bibiana Ateh11, Daniel K. White12, Alexis Ogdie13, Rui Xiao1, Tuhina Neogi14 and Carla Scanzello1, 1University of Pennsylvania, Philadelphia, PA, 2VA PUGET SOUND/UNIVERSITY OF WASHINGTON, Seattle, WA, 3Washington DC VA Medical Center, Bethesda, MD, 4University of Nebraska Medical Center, Omaha, NE, 5Brown University, Philadelphia, PA, 6Drexel University, Pittsburgh, PA, 7Dartmouth College, Lebanon, NH, 8University of Oklahoma, Philadelphia, PA, 9Teachers College, Columbia University, Philadelphia, PA, 10VA Puget Sound Health Care System, Seattle, WA, 11Washington VA Medical Center, Washington, District of Columbia, 12University of Delaware, Newark, DE, 13Department of Medicine, Perelman School of Medicine at the University of Pennsylvania, Wilmington, DE, 14Boston University School of Medicine, Boston, MA

Meeting: ACR Convergence 2025

Keywords: clinical trial, corticosteroids, Osteoarthritis, Patient reported outcomes

  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print
Session Information

Date: Tuesday, October 28, 2025

Title: Abstracts: Osteoarthritis – Clinical (2621–2626)

Session Type: Abstract Session

Session Time: 3:45PM-4:00PM

Background/Purpose: Intra-articular corticosteroids are widely used for routine management of chronic pain from knee osteoarthritis (KOA), though estimates of their benefit vary widely. We aimed to quantify the short-term benefit of corticosteroid injections in reducing symptoms of KOA in a large, pragmatic, multi-site clinical trial.

Methods: This was a factorially-designed crossover randomized trial among patients with KOA across 4 Veteran Affairs Medical Centers. Participants were 40-80 years of age, had a clinical diagnosis of KOA, a Kellgren-Lawrence X-ray grade > or = 1, and a clinical indication for joint injection according to the treating provider. Participants were randomized to an incentive arm to promote physical activity, or an attention control. Within these arms, participants were further randomized to receive blinded injections with corticosteroid plus lidocaine (40 mg methylprednisolone) or lidocaine-only in a crossover design over 28 weeks. The primary outcome was the change in the Knee Osteoarthritis Outcome Score (KOOS) (range 0-100). A change of >10 was considered the minimal clinically important difference (MCID). Linear or generalized mixed-effects models were used to evaluate the effect of the corticosteroid injection over all outcomes between 2-12 weeks. We also performed a crossover analysis among 196 participants that received a second injection at week 16 (N&#3f392). Sensitivity analyses included a last-observation-carried-forward approach to account for missingness as well as sub-group analyses.

Results: Of 231 enrolled, 221 were randomized (mean age 64 years; 84% male, median K-L grade of 3). 176 (80%) had received a prior injection. Those randomized to initial corticosteroids showed no improvement in total KOOS scores compared to lidocaine-only at any time point or when evaluating all outcomes over 12-weeks [B: 1.72 (95% CI: -1.08, 4.52) p=0.23] (Figure 1a, Table 1). The probability of achieving KOOS MCID was 20.9% v. 16.8% for the lidocaine-only arm (Risk Difference [RD] = 0.041 (95% CI: -4.1, 12.3); Number Needed to Treat [NNT] = 24 (95% CI: 8, ∞). A crossover analysis comparing 196 participants to themselves demonstrated no benefit over 12-weeks [B: 0.36 (95% CI: -1.17, 1.90) p=0.29] (Figure 1b). The probability of achieving MCID was 19.7% v. 15.3% for lidocaine-only (RD=0.044 [95% CI: -0.011, 0.10]; NNT=23 [95% CI: 10, ∞]). There were no carryover effects. Results were similar for secondary outcomes, in sensitivity analysis, and across subgroups (Table 1; Figure 2). There was no interaction with the exercise incentive arm. Among those receiving both injections, only 55% correctly guessed the order of their injections. Rescue injections were infrequent (n=6 during lidocaine-only; n=7 during corticosteroid).

Conclusion: In this well-powered, blinded, pragmatic, randomized trial, corticosteroid injections provided no significant benefit over 12 weeks compared to lidocaine-only injections. These findings, in the context of the existing literature, suggest limited benefit of this commonly performed procedure in real-world practice and raise new questions about whether this intervention should be widely used for routine management of KOA symptoms.

Supporting image 1Figure 1: Changes in total KOOS (with 95% confidence intervals) in the corticosteroid plus lidocaine (purple) and lidocaine-only (green) arms over 12 weeks of follow up for A) the primary analysis between weeks 0-12, and B) the crossover analysis. An increase in KOOS indicates an improvement/reduction in KOA symptoms.

Supporting image 2Table 1: Time-averaged change from baseline among those receiving corticosteroid plus lidocaine compared to those receiving lidocaine only over all time-points between 2 and 12 weeks. The standardized effect size (or risk difference for binary outcomes) are also shown.

Supporting image 3Figure 2: Subgroup analyses for primary outcome comparing corticosteroid plus lidocaine to lidocaine-only. Point estimates and confidence intervals shown are the estimates of difference betweenc corticosteroid and lidocaine-only groups from time-averaged mixed-effects models within each subgroup of interest. Abbreviations: KL, Kellgren-Lawrence; KOOS, Knee Osteoarthritis Outcome Score; LOCF, last observation carried forward.


Disclosures: J. Baker: Amgen, 5; K. Wysham: None; M. Quinones: None; B. England: Boehringer-Ingelheim, 2, 5; K. Jin: None; M. Olave: None; S. Wetzel: None; R. Gillcrist: None; C. Lavery: None; N. Keller: None; K. Hayes: None; B. Kramer: None; H. Brubeck: None; B. Ateh: None; D. White: None; A. Ogdie: AbbVie, 5, Amgen, 5, 11, Bristol Myers Squibb, 5, Celgene, 5, CorEvitas, 2, Eli Lilly, 5, Novartis, 5, 11, Pfizer, 5, 11; R. Xiao: None; T. Neogi: None; C. Scanzello: COMPOSITIONS AND METHODS FOR TREATING OSTEOARTHRITIS USING A CD14 INHIBITOR, 10.

To cite this abstract in AMA style:

Baker J, Wysham K, Quinones M, England B, Jin K, Olave M, Wetzel S, Gillcrist R, Lavery C, Keller N, Hayes K, Kramer B, Brubeck H, Ateh B, White D, Ogdie A, Xiao R, Neogi T, Scanzello C. Results of Large Multi-Site Pragmatic Clinical Trial Comparing Corticosteroids or Blinded Lidocaine-only Injections in Treating Osteoarthritis of the Knee [abstract]. Arthritis Rheumatol. 2025; 77 (suppl 9). https://acrabstracts.org/abstract/results-of-large-multi-site-pragmatic-clinical-trial-comparing-corticosteroids-or-blinded-lidocaine-only-injections-in-treating-osteoarthritis-of-the-knee/. Accessed .
  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print

« Back to ACR Convergence 2025

ACR Meeting Abstracts - https://acrabstracts.org/abstract/results-of-large-multi-site-pragmatic-clinical-trial-comparing-corticosteroids-or-blinded-lidocaine-only-injections-in-treating-osteoarthritis-of-the-knee/

Advanced Search

Your Favorites

You can save and print a list of your favorite abstracts during your browser session by clicking the “Favorite” button at the bottom of any abstract. View your favorites »

Embargo Policy

All abstracts accepted to ACR Convergence are under media embargo once the ACR has notified presenters of their abstract’s acceptance. They may be presented at other meetings or published as manuscripts after this time but should not be discussed in non-scholarly venues or outlets. The following embargo policies are strictly enforced by the ACR.

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of our scientific journal, Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. In an exception to the media embargo, academic institutions, private organizations, and companies with products whose value may be influenced by information contained in an abstract may issue a press release to coincide with the availability of an ACR abstract on the ACR website. However, the ACR continues to require that information that goes beyond that contained in the abstract (e.g., discussion of the abstract done as part of editorial news coverage) is under media embargo until 10:00 AM CT on October 25. Journalists with access to embargoed information cannot release articles or editorial news coverage before this time. Editorial news coverage is considered original articles/videos developed by employed journalists to report facts, commentary, and subject matter expert quotes in a narrative form using a variety of sources (e.g., research, announcements, press releases, events, etc.).

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying colleagues, institutions, communications firms, and all other stakeholders related to the development or promotion of the abstract about this policy. If you have questions about the ACR abstract embargo policy, please contact ACR abstracts staff at [email protected].

Wiley

  • Online Journal
  • Privacy Policy
  • Permissions Policies
  • Cookie Preferences

© Copyright 2025 American College of Rheumatology