RecruitingNCT07672418

Postoperative Pain After Pediatric Adenotonsillectomy With Ketorolac or Ibuprofen

Assessment of Postoperative Pain Outcomes Following Pediatric Adenotonsillectomy and the Impact on Non-Steroidal Anti-Inflammatory Drugs


Sponsor

Baylor College of Medicine

Enrollment

200 participants

Start Date

Jun 24, 2026

Study Type

OBSERVATIONAL

Conditions

Summary

This prospective observational study will evaluate postoperative pain after outpatient pediatric adenotonsillectomy in adolescents prescribed either acetaminophen with ibuprofen or acetaminophen with oral ketorolac after discharge, based on the prescribing preference of the otolaryngology surgeon. Participants will complete text-message surveys after discharge to assess pain severity, medication administration, and functional recovery for up to 14 days.


Eligibility

Min Age: 13 YearsMax Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a new treatment for people with pediatrics, sleep, and other related conditions. The study is currently recruiting participants at 1 location. People eligible for this study include aged 13 Years to 18 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Locations(1)

Baylor College of Medicine/ Texas Childrens Hospital

Houston, Texas, United States

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NCT07672418


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