Clinical Trials Directory

Trials / Unknown

UnknownNCT02152787

Comparison of Propofol 1mg/kg and Propofol 0.5mg/kg for Prevention of Emergence Agitation in Children Undergoing Strabismus Surgery During Sevoflurane Anesthesia

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
90 (estimated)
Sponsor
Yonsei University · Academic / Other
Sex
All
Age
3 Years – 12 Years
Healthy volunteers
Not accepted

Summary

The occurrence of emergence agitation (EA) in pediatric patients who have received sevoflurane anesthesia is a common postoperative problem. Among various strategies for reducing the incidence and severity of EA, the use of pharmacological agents at the end of anesthesia is thought to be the most convenient and easily applicable method in clinical situation. The one of typical agents that can be administered in this way is propofol. Previous studies demonstrated that the use of propofol 1mg/kg at the end of anesthesia could reduce the incidence of EA with low incidence of postoperative nausea and vomiting. However, it was also demonstrated that the use of propofol 1mg/kg at the end of anesthesia could delay the emergence time. The purpose of this study is to compare the preventive effect on EA and the emergence time between propofol 1mg/kg and propofol 0.5mg/kg administered at the end of sevoflurane anesthesia.

Conditions

Interventions

TypeNameDescription
DRUGInjection of propofol 1.0mg/kg
DRUGpropofol 0.5mg/kg
DRUGnormal saline

Timeline

Start date
2014-05-01
Primary completion
2015-12-01
Completion
2016-01-01
First posted
2014-06-02
Last updated
2014-07-09

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT02152787. Inclusion in this directory is not an endorsement.