Controlled Propofol Administration

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

Status

Completed

Phases

Phase 4

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT01019746

Enrollment

Registered

2009-11-25

Start date

2007-08-31

Completion date

Unknown

Last updated

2009-11-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HYPNOSIS

Keywords

Hypnosis with propofol

Brief 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.

Interventions

DRUGpropofol

propofol administration

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

TREATMENT

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to 90 Years

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

Design outcomes

Primary

Measure	Time frame
Comparison of control administration of propofol with manual administration.	1 year

Secondary

Measure	Time frame
Emergence from anesthesia	1 year

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026