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