Cardiff University | Prifysgol Caerdydd ORCA
Online Research @ Cardiff 
WelshClear Cookie - decide language by browser settings

Different dosing regimens for chronic knee osteoarthritis (KOA) pain management: A pooled analysis on celecoxib

Choy, Ernest ORCID: https://orcid.org/0000-0003-4459-8609, Fuggle, Nicholas, Biesheuvel, Egbert, Venugopal, Srinivasan, Kumbhar, Sagar Suresh, Chiaese, Raffaella Maria Rita, Walker, Chris and Reginster, Jean-Yves 2026. Different dosing regimens for chronic knee osteoarthritis (KOA) pain management: A pooled analysis on celecoxib. Aging Clinical and Experimental Research 38 (1) , 55. 10.1007/s40520-025-03302-2

[thumbnail of 40520_2025_Article_3302.pdf] PDF - Published Version
Available under License Creative Commons Attribution.

Download (1MB)

Abstract

Background: Celecoxib is widely used for the management of different chronic musculoskeletal conditions including osteoarthritis (OA), but the comparative effectiveness of 200 mg once daily (OD) versus 100 mg twice daily (BID) in patients with varying baseline pain severity is not fully established. Aims: To compare the efficacy of celecoxib 200 mg OD and 100 mg BID in reducing pain among OA patients with moderate or severe baseline pain, using pooled post hoc analyses of two similar randomized controlled trials. Materials and methods: Data from two 6-week, double-blind, placebo-controlled trials in knee OA (n = 1,360) were pooled. Patients were stratified into moderate (VAS 40–69 mm, n = 675) or severe (VAS ≥ 70 mm, n = 685) pain subgroups. Interventions included celecoxib 100 mg BID, celecoxib 200 mg OD, or placebo. Primary endpoint was change from baseline in VAS pain at weeks 2 and 6, analyzed via mixed-effects model for repeated measures (MMRM) and ANCOVA with last observation carried forward. WOMAC pain score was a secondary endpoint. Results: Both celecoxib regimens significantly reduced VAS pain scores versus placebo at weeks 2 and 6 in the overall and moderate pain groups (p < 0.05). In severe pain patients, both regimens were superior to placebo at week 2; however, at week 6, only the 200 mg OD regimen retained statistical significance (LS mean difference vs. placebo − 7.45, p = 0.0135), while 100 mg BID did not. WOMAC pain score results mirrored VAS findings, with 200 mg OD showing the greatest improvement in severe baseline pain. Conclusion: Celecoxib 100 mg BID and 200 mg OD are both effective for OA pain relief, in moderate and severe pain. Findings suggest 200 mg OD may confer an advantage in patients with severe baseline pain in the long-term treatment (week 6).

Item Type: Article
Date Type: Published Online
Status: Published
Schools: Schools > Medicine
Additional Information: License information from Publisher: LICENSE 1: URL: http://creativecommons.org/licenses/by/4.0/, Type: open-access
Publisher: Springer
ISSN: 1594-0667
Date of First Compliant Deposit: 4 February 2026
Date of Acceptance: 18 December 2025
Last Modified: 04 Feb 2026 10:45
URI: https://orca.cardiff.ac.uk/id/eprint/184396

Actions (repository staff only)

Edit Item Edit Item

Downloads

Downloads per month over past year

View more statistics