CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 99 enrolled
Drug / intervention
Propofoldrug
Likely dose
Propofol 0.1 mlfrom 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/NCT00535613
NCT00535613Phase 4Completed
CompareCT.gov

Does a Single Dose of Propofol Decrease the Incidence of Emergence Agitation in Children?

University of Wisconsin, Madison·interventional·Posted Sep 26, 2007·Updated Oct 21, 2019

In Brief

A Phase 4 clinical trial evaluating Propofol for Emergence Agitation. Completed, enrolled 99 participants across 1 site.

Detailed Summary

The purpose of the study is to see if a small dose of propofol given intravenously (through a needle into a vein) at the end of anesthesia can make it less likely that children will be agitated as the come out of the anesthetic.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsEmergence Agitation
CountriesUnited States
Collaborators--

Timeline

Phase 4CompletedFinished
20082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedSep 26, 2007
Enrollment StartAug 1, 2007
Primary CompletionDec 1, 2010
TodayJul 2, 2026
Enrollment to primary: 3.3 yearsPosted 18.8 years ago

Interventions

Propofoldrug

IV, single bolus at completion of anesthetic, 0.1 ml/kg