Overview

A Phase IV Study Investigating the Effects of Remifentanil Concentrations on Propofol Requirements for Loss of Consciousness, Response to Painful Stimuli, Bispectral Index and Associated Haemodynamic Changes

Status:
Completed

Trial end date:
2015-08-01

Target enrollment:

Participant gender:

Summary

A prospective, randomised, phase IV trial including 150 patients. To evaluate the effects of varied concentrations of remifentanil on the proposal requirements for the loss of consciousness and response to pain and to evaluate the haemodynamic changes and processed EEG (BIS) during induction of anaesthesia.

Phase:

Phase 4

Details

Lead Sponsor:

The University of Hong Kong

Treatments:

Propofol
Remifentanil