Dexmedetomidine for Continuous Sedation

Status Terminated

Clinical Trial 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.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment

Related Conditions & MeSH terms

Conscious Sedation

Clinical Trial Details

NCT number	NCT00226785
Study type	Interventional
Source	Orion Corporation, Orion Pharma
Contact
Status	Terminated
Phase	Phase 3
Start date	October 2005
Completion date	July 2006

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See also
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