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Clinical Trial Summary

The purpose of this study is to assess efficacy and safety of dexmedetomidine at the time of extubation and after extubation, in patients requiring postoperative sedation in the ICU.


Clinical Trial Description

The study is to conduct as a phase IV post-marketing clinical study in accordance with the approval condition of dexmedetomidine hydrochloride in Japan. The study will compare the use of dexmedetomidine in patient management at the time of extubation with other sedative/ analgesic management, Comparison is made in the use of dexmedetomidine in patient management between a group in which management is performed with dexmedetomidine and a group in which standard management is performed with propofol in patients requiring postoperative sedation in the ICU The usefulness of dexmedetomidine during postextubation period is also evaluated. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00318955
Study type Interventional
Source Hospira, now a wholly owned subsidiary of Pfizer
Contact
Status Completed
Phase Phase 4
Start date November 2005
Completion date August 2006

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