drugset / Trial / NCT02832687
Multi-dose Acetaminophen for Patients Undergoing General Anesthesia
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Acetaminophen | Small molecule | 12.5 mg/kg | Intravenous |
| Subject | Acetaminophen | Small molecule | 1000 mg | Intravenous |