Clinical trial
Target-controlled Infusion of Propofol and Remifentanil for Postoperative…
NCT00393003 · Hopital Foch, Other · Completed
Key facts
| NCT number | NCT00393003 |
|---|---|
| Title | Target-controlled Infusion of Propofol and Remifentanil for Postoperative Sedation Guided by the Bispectral Index |
| Official title | Target-controlled Infusion of Propofol and Remifentanil for Postoperative Sedation Guided by the Bispectral Index: Comparison Between Manual Perfusion and Automated Perfusion |
| Lead sponsor | Hopital Foch, Other |
| Status | Completed |
| Phase | Phase 4 |
| Study type | Interventional |
| Conditions | Postoperative Sedation |
| Intervention type | Device |
| Interventions | Closed-loop anesthesia system |
| Enrollment | 32 |
| Start date | Sep 1, 2006 |
| Primary completion | Apr 1, 2007 |
| Completion | Apr 1, 2007 |
| First posted | Oct 26, 2006 |
| Last update posted | Aug 31, 2009 |
| Countries | France |
At a glance
- 1–9 Study sites
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: