NCT07576985
Evaluating the Efficacy of Intravenous Acetaminophen (IV Tylenol) in Reducing Pain and Agitation in Pediatric Patients Undergoing Elective Tonsillectomy and/or Adenoidectomy
Enrolling by Invitation
Not specifiedUp to 8ObservationalMetroHealth Medical CenterInvestigator-initiated
~20 participants
Updated 2026-05-08 on ClinicalTrials.gov
What's tested:No Intervention: Observational Cohort
At a glance
Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Pain Assessment
Measured over * "Baseline" * "Perioperative/Periprocedural"
Conditions
Where it's being run
1 sites across 1 statesOhio1
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
Do you actually qualify for this trial?
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Eligibility criteria
Inclusion
Subjects pediatric patients aged ≤7 years, observed by study team who will complete the scales
Undergoing elective tonsillectomy and adenoidectomy.
Exclusion
Pre-existing neurological or developmental disorders impacting pain/agitation scores
What this trial measures
- Pain Assessment* "Baseline" * "Perioperative/Periprocedural"
Evaluate the impact of IV Acetaminophen on pain at emergence and in the Post-Anesthesia Care Unit (PACU) using a validated pediatric assessment tool, FLACC (Face, Legs, Activity, Cry, Consolable) Behavior Pain Assessment Tool.