Comparing Analgesic Regimen Effectiveness and Safety for Surgery for Kids Trial
NCT06671002
This study is recruiting at 4 US sites in 3 states, according to its ClinicalTrials.gov record last updated .
Summary
This trial is being completed to compare two commonly used options to treat pain after discharge from surgery. Participants that undergo tonsil removal, gallbladder removal, and knee scope will be eligible to enroll. Eligible participants will be randomized to prescription of 1 of 2 groups of medications (Non-Steroidal Anti-Inflammatory Drugs (NSAIDs) plus acetaminophen or low dose opioids with the NSAIDs plus acetaminophen. The key question the study seeks to answer is which option will have the best outcomes and with the fewest side effects?
Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov
Conditions studied
- Surgery
- Pain, Post Operative
Eligibility basics and study details
- Study type
- Interventional
- Phase
- Phase 4
- Ages
- 12 to 20 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Sponsor
- University of Michigan
- Last updated on ClinicalTrials.gov
- March 4, 2026
These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.
US recruiting sites
California · 2
- Children's Hospital Los Angeles (CHLA) · Los Angeles, CA
- Lucile Packard Children's Hospital Stanford · Palo Alto, CA
Michigan · 1
- University of Michigan · Ann Arbor, MI
Ohio · 1
- Nationwide Children's (NCH) · Columbus, OH
Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.