Controlled Propofol Administration

• Status: Completed
• Trial end date: 1969-12-31
• Target enrollment: 0
• Participant gender: All

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.

• Phase: Phase 4
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: McGill University Health Center; McGill University Health Centre/Research Institute of the McGill University Health Centre
• Treatments: Propofol

Criteria

Inclusion Criteria:

• patients aged 18 to 90 years

• surgery lasting more than 30 min

Exclusion Criteria:

• inability to provide informed consent

• allergies to study drug