Trials / Completed
CompletedNCT01019746
Controlled Propofol Administration
Comparison of Closed-oop of Propofol Versus Manual Control Using Bispectral Index (BIS)
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 40 (estimated)
- Sponsor
- McGill University Health Centre/Research Institute of the McGill University Health Centre · Academic / Other
- Sex
- All
- Age
- 18 Years – 90 Years
- Healthy volunteers
- Not accepted
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | propofol | propofol administration |
Timeline
- Start date
- 2007-08-01
- Primary completion
- 2008-05-01
- First posted
- 2009-11-25
- Last updated
- 2009-11-25
Locations
1 site across 1 country: Canada
Source: ClinicalTrials.gov record NCT01019746. Inclusion in this directory is not an endorsement.