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Clinical Trial Summary

The purpose of the study is to determine the efficacy of IV acetaminophen when administered to neurosurgical patients at the beginning and end of their surgery. If the result is improved pain control with less opioid consumption postoperatively, then those patients may also experience less opioid related side effects such as nausea/vomiting, pruritus, and sedation. While numerous other studies have failed to show a benefit of IV acetaminophen after neurosurgical procedures, we are studying the administration of 1 g in two doses over the course of the operation.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03445390
Study type Interventional
Source Stanford University
Contact
Status Completed
Phase Phase 4
Start date May 1, 2014
Completion date November 1, 2017

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