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Clinical Trial Summary

The bispectral index parameter is used to guide the titration of general anesthesia, however; conflicting results between different studies cannot prove the benefit of EEG monitor on improvement of OR efficiency. Next Generation SedLine features an enhanced signal processing engine, which provides processed EEG parameters. This four channel EEG monitor for the monitoring of perioperative anesthesia depth prevent overdose of medication and may help for individualized anesthetic plan. This research intended to observe the emergence time from end of the surgical wound closure to patient awake (or to extubation) with or without SedLine.

Clinical Trial Description

This is a clinical observation study. Inclusion criteria are patients with ASA 1-3, age over 20 who need general anesthesia surgery without other neurologic disease. All inclusions will receive the general anesthesia with SedLine monitor, a researcher who is not participated in the clinical practice will record the emergence characters and the EEG monitor signal. The Controls were patients with same criteria without BIS monitor. Sample size was decided if the estimated difference between SedLine group and BIS group are 1 minute and the average estimated as 2 minute. With 80% desired power and default is .05, each group will need 63 cases. ;

Study Design

Related Conditions & MeSH terms

  • Drug-Related Side Effects and Adverse Reactions
  • General Anesthetic Drug Adverse Reaction
  • Perioperative/Postoperative Complications
  • Postoperative Complications

NCT number NCT05208502
Study type Observational
Source National Taiwan University Hospital
Contact Feng-Fang Tsai
Phone 886-2-3123456
Status Recruiting
Start date February 22, 2022
Completion date December 31, 2024

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