Celecoxib for ENT Pain Management
Part of paid clinical trials in Madison, Wisconsin.
- Sponsor
- University of Wisconsin, Madison
- Study ID
- NCT06505187
- Phase
- PHASE2
- Status
- Recruiting
Conditions
- Parotidectomy
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Celecoxib — DRUG200mg every 12 hours
- Tylenol — DRUG650mg q6h
- Oxycodone — DRUG5mg every 6 hours as needed
- placebo — DRUGevery 12 hours
Study Details
The goal of this clinical trial is to find out whether pain can be managed after an operation with celecoxib instead of oxycodone. The main question it aims to answer is if use of celecoxib plus Tylenol reduces the need for oxycodone. Researchers will compare the combination of celecoxib and Tylenol to a placebo to find out whether celecoxib works to manage pain. Participants will: * Take celecoxib, or a placebo, plus Tylenol with opioids as needed * Keep a diary of their pain between visits * Complete questionnaires
Key Dates
- Start date
- Feb 28, 2025
- Status verified
- Dec 2025
- Primary completion
- Sep 30, 2026
- Completion
- Sep 30, 2026
Study Design
- Enrollment
- 84 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- SUPPORTIVE_CARE
Arms
- Experimental: Celecoxib for pain managementParticipants receive celecoxib in addition to Tylenol and oxycodone
- Sham Comparator: Placebo for pain managementParticipants receive placebo in addition to Tylenol and oxycodone
Primary Outcome Measure
Number of oxycodone pills taken [ Time Frame: 7 days ]
Central Contacts
- Hayley Mann, MD480-272-4258
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of Wisconsin | Madison | Wisconsin | 53702 |
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