Atlas Trials

Target-controlled Infusion of Propofol and Remifentanil for Postoperative Sedation Guided by the Bispectral Index

Clinical trial NCT00393003 · COMPLETED

Trial details

NCT number
NCT00393003
Sponsor
Hopital Foch
Status
COMPLETED
Phase
Phase 4
Study type
INTERVENTIONAL
Postoperative Sedation
Start date
2006-09-01
Primary completion
2007-04-01
Enrollment
32

View on ClinicalTrials.gov

Track trials programmatically

Sponsors, conditions and status changes through the Atlas API.