Controlled Propofol Administration

Phase 4CompletedNCT01019746

McGill University Health Centre/Research Institute of the McGill University Health Centre40 enrolled

Overview

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.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

HYPNOSIS

Interventions

propofolDRUG

propofol administration

Eligibility

Sex: ALLMin age: 18 YearsMax age: 90 Years

Medical Language ↔ Plain English

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

Locations (1)

MUHC - Montreal General Hospital

Montreal, Quebec, Canada

Outcomes

Primary Outcomes

Comparison of control administration of propofol with manual administration.

Time frame: 1 year

Secondary Outcomes

Emergence from anesthesia

Time frame: 1 year

Data from ClinicalTrials.gov

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