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NOT YET RECRUITING
NCT07079969
PHASE2

Effects of Photobiomodulation and Topical Diclofenac on Inflammation and Pain in Knee Osteoarthritis (EPIC-KO)

Sponsor: University of Florida

View on ClinicalTrials.gov

Summary

This study aims to compare the effects of combined treatments-dual-wavelength photobiomodulation (PBM) with or without topical diclofenac-on inflammation, pain, and joint function in patients with knee osteoarthritis (OA). It also seeks to determine the synergistic effect of PBM plus topical diclofenac on inflammatory markers, pain scores, and functional outcomes.

Official title: Effects of Photobiomodulation and Topical Diclofenac on Inflammation and Pain in Knee Osteoarthritis

Key Details

Gender

All

Age Range

50 Years - 99 Years

Study Type

INTERVENTIONAL

Enrollment

32

Start Date

2026-04

Completion Date

2026-07

Last Updated

2026-02-27

Healthy Volunteers

No

Interventions

DEVICE

Photobiomodulation therapy (PBM) device

FDA-cleared near-infrared PBM device delivering therapeutic light to the affected knee. Administered once per session, approximately 10 minutes after topical application, in six sessions over 2-3 weeks (2-3 times per week).

DEVICE

Sham PBM device

Identical in appearance to the active PBM device but emits no therapeutic light. Administered once per session, approximately 10 minutes after topical application, in six sessions over 2-3 weeks.

DRUG

Diclofenac Sodium 1 % Topical Cream

Topical nonsteroidal anti-inflammatory drug applied at a dose of 4 grams to the affected knee, once per session, immediately before PBM/sham PBM. Used in six sessions over 2-3 weeks.

DRUG

Placebo topical cream

Inert cream matching the appearance of diclofenac sodium 1% gel. Applied at 4 grams to the affected knee, once per session, immediately before PBM/sham PBM. Used in six sessions over 2-3 weeks

Locations (1)

University of Florida

Gainesville, Florida, United States