Target-controlled Infusion of Propofol and Remifentanil for Postoperative Sedation Guided by the Bispectral Index
This study has been completed.
Sponsor:
Hopital Foch
Information provided by:
Hopital Foch
ClinicalTrials.gov Identifier:
NCT00393003
First received: October 24, 2006
Last updated: August 28, 2009
Last verified: August 2009
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No Study Results Posted on ClinicalTrials.gov for this Study
| Study Status: | This study has been completed. |
|---|---|
| Study Completion Date: | April 2007 |
| Primary Completion Date: | April 2007 (Final data collection date for primary outcome measure) |