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Clinical Trial Summary

The aim of this study is to increase knowledge about drug properties and effects during therapeutic hypothermia. The primary end point of this study is the time from termination of sedation to extubation in patients treated with therapeutic hypothermia, after treatment with the combination remifentanil and propofol versus that of fentanyl and midazolam.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT00667043
Study type Interventional
Source Norwegian University of Science and Technology
Contact
Status Completed
Phase Phase 4
Start date April 2008
Completion date June 2010

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