Non-Opioid Pain Medications After Intracapsular Adenotonsillectomy
Adenotonsillectomy, Post-operative Analgesia, Opioid Use
About this trial
This is an interventional treatment trial for Adenotonsillectomy focused on measuring analgesia, pain control, adenotonsillectomy, tonsillectomy, opioids, post-operative pain, intracapsular
Eligibility Criteria
Inclusion Criteria:
• Patients age 3 - 17 undergoing adenotonsillectomy
Exclusion Criteria:
- Down syndrome
- History of coagulopathy
- Craniofacial abnormalities other than plagiocephaly or submucous cleft palate (SMCP)
- Caregivers who cannot speak, read, or write in English proficiently
- Patients who take opioids during the enrollment period
- Patients who take chronic opioids
- Pregnancy
- Allergy to or contraindication for taking any of the study medications
- Patients who have the inability to communicate
- Patients who have the inability to localize pain
Sites / Locations
- UPMC Children's Hospital of PittsburghRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Experimental
Active Comparator
Opioid pain control
Opioid pain control + Disposal Pouch
Non-opioid pain control
Patients in this group will be receiving triple therapy for pain control with oxycodone, acetaminophen, and ibuprofen. They will be asked to complete a pain diary which will be used to determine the level of pain control achieved with this regimen. The diary will be completed by post-operative day 14. A post-operative appointment between 4-8 weeks will be scheduled and the patient and caregiver will return the pain diary or by email/mail if no appointment was scheduled. Families will receive an opioid disposal education document.
Patients in this group will be receiving triple therapy for pain control with oxycodone, acetaminophen, and ibuprofen. They will be asked to complete a pain diary which will be used to determine the level of pain control achieved with this regimen. The diary will be completed by post-operative day 14. A post-operative appointment between 4-8 weeks will be scheduled and the patient and caregiver will return the pain diary or by email/mail if no appointment was scheduled. Half of the families randomized to the opioid group will be further randomized to receive an opioid disposal bag + an opioid disposal education document. The pouch is a drug deactivation disposal pouch to dispose the opioid at home.
Patients in this group will be receiving therapy for pain control with acetaminophen and ibuprofen only. They will be asked to complete a pain diary which will be used to determine the level of pain control achieved with this regimen. The diary will be completed by post-operative day 14. A post-operative appointment between 4-8 weeks will be scheduled and the patient and caregiver will return the diary or by email/mail if no appointment was scheduled.