The Effects of Patient and Visit Characteristics on Health Outcomes in Knee Osteoarthritis
Part of paid clinical trials in Sacramento, California.
- Sponsor
- University of California, Davis
- Study ID
- NCT06574191
- Status
- Recruiting
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 50 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Topical Diclofenac gel 1% — DRUGTopical NSAID
Study Details
The goal of this clinical trial is to understand the patient and clinic visit characteristics that affect health outcomes for individuals with knee osteoarthritis (OA) pain using topical diclofenac gel. The main questions it aims to answer are: * What baseline patient characteristics predict response to topical diclofenac? * Does patient physiology during the study visit predict response to topical diclofenac? * Do study visit characteristics predict response to topical diclofenac? Participants will: * attend 2 study visits to complete study questionnaires and have blood drawn * apply topical diclofenac to their knee for 8 weeks * complete biweekly questions about knee pain and diclofenac use between study visits
Key Dates
- Start date
- Jan 29, 2025
- Status verified
- Mar 2026
- Primary completion
- Jan 27, 2028
- Completion
- Jan 27, 2028
Study Design
- Enrollment
- 220 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- BASIC_SCIENCE
Arms
- Experimental: DiclofenacAll study participants receiving topical diclofenac gel 1%. Participants will be instructed to apply 4 grams of the gel to the index knee at least once per day, and up to 4 times per day, for 8 weeks.
Primary Outcome Measure
Knee Pain [ Time Frame: 8 weeks ]
Central Contacts
- Maya Porter916-734-4216
- Michelle Dossett, MD, PhD916-734-5367
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of California Davis Health | Sacramento | California | 95817 |
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