drugset / Trial / NCT00226785

Dexmedetomidine for Continuous Sedation

NCT00226785

Phase 3 Terminated 900 enrolled Orion Corporation, Orion Pharma
RandomizedParallel-groupDouble-blindTreatment

Summary

The study aims to demonstrate that dexmedetomidine is non-inferior to current best practice sedation with propofol/midazolam and daily sedation stops, in maintaining a target depth of sedation in long-stay intensive care unit (ICU) patients, and that dexmedetomidine, compared with current best practice, reduces the length of ICU stay.

Timeline

Start
2005-10
Primary completion
Completion
2006-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Dexmedetomidine Other / unclassified 1.4 ug/kg Intravenous

Indications

No indication recorded.