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Not Yet Recruiting NCT07672418

Postoperative Pain After Pediatric Adenotonsillectomy With Ketorolac or Ibuprofen

Conditions: Sleep, Pediatrics, Adenotonsillectomy

Sex: All
Ages: 13 Years – 18 Years
Healthy volunteers: No
Enrollment: 200
Sponsor: Baylor College of Medicine

Location: Baylor College of Medicine/ Texas Childrens Hospital Houston Texas

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 Criteria

Inclusion Criteria: Scheduled for outpatient adenotonsillectomy Age 13-18 years ASA physical status I-III Patient or parent has access to a phone with text-messaging capability Patient assent Parent or legal guardian consent Exclusion Criteria: Inpatient admission or planned 23-hour observation Known hematologic condition or prior bleeding disorder Current anticoagulant use Known or suspected chronic kidney disease or solitary kidney Known or suspected liver disease or prior liver transplant Known or suspected mitochondrial disease or genetic anomaly Inability to self-report pain History of gastrointestinal ulcer or bleeding Allergy to acetaminophen, ibuprofen, or ketorolac Non-English or non-Spanish speaking Chronic pain or condition requiring frequent routine NSAID use Patient refusal Parent or guardian refusal

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07672418). StuddyBuddy aggregates publicly available trial information.