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Controlled Propofol Administration

HYPNOSIS Clinical Trial

Official title:
Comparison of Closed-oop of Propofol Versus Manual Control Using Bispectral Index (BIS)

Clinical Trial Summary

The purpose of this study is to compare the administration of the standard anesthetic agent (propofol) using this automatic system with the manual administration of propofol by the anesthesiologist.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01019746
Study type Interventional
Source McGill University Health Center
Contact
Status Completed
Phase Phase 4
Start date August 2007
View Details
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