Opioid Sparing Anesthesia Care for Pediatric Patients Having Tonsil Surgery
Completed · Not applicable
Conditions studied: Tonsillitis, Post-operative Nausea and Vomiting (PONV), Emergence Delirium, Opioid Analgesic Adverse Reaction, Anesthesia, Pain
In brief
This is a prospective, randomized, controlled, non-inferiority study of patients undergoing tonsil surgeries at Boston Children's Hospital Waltham. The overall aim is to evaluate the efficacy of an opioid anesthetic plan (morphine, ketorolac, and acetaminophen versus an opioid sparing anesthetic plan (dexmedetomidine, ketorolac and acetaminophen) for perioperative analgesia and recovery time in patients undergoing tonsillectomies and tonsillotomies at Boston Children's Hospital Waltham. Secondary measures include rescue opioids administered in post-anesthesia care unit (PACU), re-operation secondary to bleeding, emergence delirium, post-operative nausea and vomiting, intraoperative hemodynamics, intraoperative vasopressor administration, and length of procedure.
Key facts
- Study ID
- NCT06326983
- Run by
- Boston Children's Hospital
- People needed
- 62
- Starts
- 2024-05-09
- Expected to finish
- 2026-03-01
- Last updated by the study team
- 2026-05-18
Who can join
Age: 3 and older, up to 17. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- American Society of Anesthesia classification status I-III
- Ages 3 years to 17 years
- Scheduled for tonsillectomy or tonsillotomy with or without adenoidectomy at Boston Children's Hospital Waltham
You may not qualify if…
- Patients not scheduled for primary tonsillectomy/tonsillotomy.
- Patients with known coagulopathies
- Patients with previous chronic pain syndromes
- Patients with any condition/indication that would prevent them from being able to be randomized (i.e. allergy to one of the study medications)
Where it is running
- Boston Children's Hospital — Waltham, Massachusetts, United States
Full record on ClinicalTrials.gov
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