CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 27 enrolled
Drug / intervention
Acetaminophen +1 moredrug
Likely dose
Acetaminophen 1 gfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03445390
NCT03445390Phase 4Completed

The Effect of Intravenous Acetaminophen on Post-Operative Pain After Craniotomy: A Randomized Control Trial

Stanford University·interventional·Posted Feb 26, 2018·Updated Mar 1, 2019

In Brief

A Phase 4 clinical trial evaluating Acetaminophen and Placebo for Pain. Completed, enrolled 27 participants across 1 site.

Detailed 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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPain
CountriesUnited States
Collaborators--

Timeline

Phase 4CompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedFeb 26, 2018
Enrollment StartMay 1, 2014
Primary CompletionOct 1, 2017
Study CompletionNov 1, 2017
TodayJul 2, 2026
Enrollment to primary: 3.4 yearsPosted 8.3 years ago

Interventions

Acetaminophendrug

Acetaminophen 1 g intravenous given at the beginning and end of surgery.

Placebodrug

Placebo to match acetaminophen given at the beginning and end of surgery.