Effect Site Controlled, Reaction Time Safeguarded, Patient Maintained Sedation With Propofol in Healthy Volunteers
This study has been completed.
Sponsor:
Sonia Allam
Collaborator:
NHS Greater Glasgow and Clyde
Information provided by (Responsible Party):
Sonia Allam, University of Glasgow
ClinicalTrials.gov Identifier:
NCT00321360
First received: May 1, 2006
Last updated: February 4, 2012
Last verified: February 2012
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No Study Results Posted on ClinicalTrials.gov for this Study
| Study Status: | This study has been completed. |
|---|---|
| Study Completion Date: | September 2006 |
| Primary Completion Date: | September 2006 (Final data collection date for primary outcome measure) |