Efficacy of PLEM100(Inbody®) in Children

Status Completed

Clinical Trial Summary

Evaluation of efficacy of PLEM100(Inbody®) in measuring the sedation level in pediatric patients

Clinical Trial Description

The investigators plan to gather the basic data relevant to measurement of the level of consciousness/sedation in pediatric patients with developing brain by using PLEM100(Inbody®)

PLEM100 (Inbody®) is a medical equipment to measure, based on phase lag entropy algorithm, the level of patient consciousness, which is expressed by PLE score ranging from 0 (burst suppression or deep sedated) to 100 (awake).

In this study, pediatric patients aged from 3 to 6 years old who undergo total intravenous general anesthesia are chosen as target subjects. The investigators measure how PLE score changes during 1) anesthesia induction, 2) anesthesia maintenance, 3) emergence from anesthesia. Then, the PLE score would be validated by analyzing the correlation with the consciousness level expressed in University of Michigan Sedation Scale (UMSS). ;

Study Design

Related Conditions & MeSH terms

Development, Child

Clinical Trial Details

NCT number	NCT03195686
Study type	Observational
Source	Seoul National University Hospital
Contact
Status	Completed
Phase
Start date	August 15, 2017
Completion date	July 30, 2018

View Details

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