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Clinical Trial Summary

The primary objective of this study is to determine the noninferiority of inhaled loxapine compared to intramuscular haloperidol/lorazepam on agitation reduction at 120 minutes.


Clinical Trial Description

The primary objective of this study is to determine the noninferiority of inhaled loxapine compared to intramuscular haloperidol/lorazepam on agitation reduction at 120 minutes. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03110900
Study type Interventional
Source University of Arkansas
Contact
Status Terminated
Phase Phase 4
Start date September 30, 2017
Completion date April 4, 2018

See also
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