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Bispectral Index and End-Tidal Anesthetic Gas Concentration in Pediatric Patients — BTIGER  

Anesthesia Clinical Trial

Official title:
Bispectral Index and End-Tidal Anesthetic Gas Concentration in Pediatric Patients Undergoing Sevoflurane Anesthesia (BTIGER)

Clinical Trial Summary

The purpose of this study is to investigate the relationship between BIS™ values including EEG profile and anesthetic agents in the pediatric population

Clinical Trial Description

This is a multi-center, prospective, observational, non-invasive, randomized controlled study to collect data to compare the performance of standard practice (SP) group with the BIS™ monitoring (BIS) group. Pediatric patients between the ages of 4 to 18 years undergoing routine sevoflurane general anesthesia with an expected surgical procedure duration of greater than 30 minutes will be recruited. If the surgery is less than 15 minutes, the data will continue to be collected, but will not be included in the data analysis and the subject will be replaced with an additional subject. General surgeries including abdominal, urological, orthopedic, or ophthalmological procedures with an American Society of Anesthesiologists physical status of I - III. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04810481
Study type Interventional
Source Medtronic - MITG
Contact
Status Completed
Phase N/A
Start date July 2, 2021
Completion date October 12, 2022
View Details
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