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Clinical Trial Summary

Our hypothesis is that a new method of depth of anaesthesia monitoring, using theoretically based time series modelling will result in improved ability to determine nitrous oxide anaesthetic effect


Clinical Trial Description

We randomised patients to 0% 33% or 66% nitrous oxide during sevoflurane induction and measured anesthetic endpoints. ;


Study Design

Allocation: Randomized, Endpoint Classification: Pharmacodynamics Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Diagnostic


Related Conditions & MeSH terms


NCT number NCT00226837
Study type Interventional
Source Melbourne Health
Contact
Status Completed
Phase Phase 4
Start date August 2004
Completion date August 2005

See also
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Completed NCT00455026 - Effect of Remifentanil on Electroencephalographic BAR Index During Propofol Anaesthesia Phase 1
Completed NCT03209323 - Epileptiform EEG Patterns During Induction of General Anaesthesia With Sevoflurane Compared to Those With Propofol N/A