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 — DRUG
    200mg every 12 hours
  • Tylenol — DRUG
    650mg q6h
  • Oxycodone — DRUG
    5mg every 6 hours as needed
  • placebo — DRUG
    every 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 management
    Participants receive celecoxib in addition to Tylenol and oxycodone
  • Sham Comparator: Placebo for pain management
    Participants receive placebo in addition to Tylenol and oxycodone

Primary Outcome Measure

Number of oxycodone pills taken [ Time Frame: 7 days ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
University of WisconsinMadisonWisconsin53702
Hayley Mann, MD
480-272-4258

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