Clinical Trials Directory

Trials / Completed

CompletedNCT01020643

Closed-loop Sedation of Propofol for Patients Undergoing Spinal Anesthesia

Comparison of Closed-loop Control System of Propofol Versus Manual Control Using Bispectral Index for Controlled Sedation - a Pilot Study

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
203 (actual)
Sponsor
Thomas Hemmerling · 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 a standard anesthetic drug (propofol) using an automatic, expert-based system versus a manually controlled system by the anesthesiologist. In addition, the performance of the decision support system will be evaluated.

Conditions

Interventions

TypeNameDescription
DRUGcontrolled administration of propofolcomparison of propofol sedation

Timeline

Start date
2009-11-01
Primary completion
2011-08-01
Completion
2011-08-01
First posted
2009-11-25
Last updated
2013-10-25

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT01020643. Inclusion in this directory is not an endorsement.

Closed-loop Sedation of Propofol for Patients Undergoing Spinal Anesthesia (NCT01020643) · Clinical Trials Directory