Controlled Propofol Administration

McGill University

Status and phase: Completed; Phase 4

Conditions: HYPNOSIS

Treatments: Drug: propofol

Study type: Interventional

Funder types: Other

Identifiers

NCT01019746

GEN#07-002

GEN-07-002

Details and patient eligibility

About

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.

Enrollment: 40 estimated patients

Sex: All

Ages: 18 to 90 years old

Volunteers: No Healthy Volunteers

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

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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40 participants in 1 patient group

control propofol administration

Experimental group

Treatment:

Drug: propofol