drugset / Trial / NCT02832687

Multi-dose Acetaminophen for Patients Undergoing General Anesthesia

NCT02832687 ↗

RandomizedParallel-groupQuadruple-blindSupportive care

Summary

Study Objective The aim of the proposed study is to examine the effect of Q4 hour multidose IV acetaminophen on patients' readiness for discharge. In doing so the investigators will also investigate the various factors that could potentially contribute to a patient's readiness for discharge such as overall opioid consumption, time to rescue medication, incidence of postoperative nausea and vomiting, pain scores, and perioperative stress markers and their overall correlation with IV acetaminophen intake.

Timeline

Start
2017-06-19
Primary completion
2020-09-01
Completion
2020-12-31

Outcome

Outcome not reported

Stopped: “The study was halted due to the worldwide COVID-19 pandemic and the cancellation of all elective cases.”

Drugs

EvaluationDrugModalityDoseRoute
Subject Acetaminophen Small molecule 12.5 mg/kg Intravenous
Subject Acetaminophen Small molecule 1000 mg Intravenous