About this trial
This is a prospective, observational study to determine the association between preoperative fasting duration and post-tonsillectomy pain scores in the post-anesthesia care unit (PACU) among pediatric patients undergoing tonsillectomy with or without adenoidectomy and/or tympanostomy tube placement. The primary outcome is the post-tonsillectomy pain score, with the secondary outcomes as total postoperative opioid consumption, PACU length of stay, and hospital length of stay.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
undergoing elective tonsillectomy with or without adenoidectomy and/or tympanostomy tube placement
Disqualifiers
non-elective or urgent procedures
inpatient admission prior to surgery; patients with any missing required data
patients with conditions requiring deviation from standard anesthetic management (as determined by the anesthesiologist)
Trial population
Pediatric patients undergoing tonsillectomy surgery
Trial design
Cohort
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Post-tonsillectomy pain scores
Pain scores will be assessed in the post-anesthesia care unit (PACU) and on the inpatient floor (if admitted) every 15 minutes - 4 hours for the duration of their recovery until hospital discharge. The patient is asked to rate their pain on a scale of 0-10 with 0 being no pain and 10 being worst pain imaginable.
Secondary outcomes
Postoperative opioid consumption
The amount of opioid pain medication the patient received following their surgery until hospital discharge.
PACU length of stay
Amount of time between admission to the post-anesthesia care unit (PACU) and discharge from the PACU.
Hospital length of stay
Amount of time between admission to the pre-op unit prior to surgery until discharge from the hospital.
Sponsors and contacts
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Brittany Willer
Lead sponsor
Nationwide Children's Hospital
Sponsor institution
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