Knee Osteoarthritis Pain Study with Duloxetine, Celecoxib, or Placebo
This study at Northwestern University is for people with knee osteoarthritis (OA) pain. It aims to understand why some people respond to certain pain medicines and others don't. You could be eligible if you are over 40, have knee OA confirmed by X-ray, and experience knee pain most days, with an average pain score of 4 or higher out of 10. The study will last about 20 weeks. You will be randomly assigned to receive either duloxetine, celecoxib, or a placebo (an inactive pill). Researchers will measure how many people have at least a 30% reduction in their pain after 6 and 16 weeks of treatment. The study is currently unclear about its recruitment status and plans to enroll 180 participants.
- Study design
- This is an interventional study where 180 participants will be randomly assigned to one of three treatment groups: duloxetine, celecoxib, or placebo. The study design involves a repeat-treatment approach.
- What's involved
- You would participate for about 20 weeks, have a knee X-ray, optional brain and knee MRIs, blood draws, pain sensitivity tests, and complete questionnaires.
- Compensation
- Not stated in the trial record.
- Follow-up
- Pain response will be measured at the end of the first treatment period (week 6) and the second treatment period (week 16).
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Brain-Based and Clinical Phenotyping of Pain Pharmacotherapy in Knee Osteoarthritis
At a glance
Conditions
NCT06245109
Where you'd take part
This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
Northwestern University
Chicago, Illinoisstudy coordinator listed
Recruiting
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Study leadership
- Thomas J Schnitzer, MD, PhD · PRINCIPAL_INVESTIGATOR · Northwestern University
Who to contact
Opens a ready-to-send draft in your own email app — review before sending.
What this trial measures
- Percentage of Individuals with at least 30% Pain Response to treatmentBaseline to end of first treatment period (week 6) and second treatment period (week 16)
At least 30% improvement from baseline in "weekly average daily pain" measured using a numeric rating scale (0-10) with 0 = no pain and 10 = worst pain