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Clinical Trial Summary

Intranasal dexmedetomidine has shown to be an effective sedative when used prior to anaesthetic induction as premedication. 1mcg/kg intranasal dexmedetomidine was used in previous study and it produced satisfactory sedation in more than 50% of the children at the time of anaesthetic induction with no adverse effect. In this study we aim to compare 1mcg/kg with 2mcg/kg intranasal dexmedetomidine in children. We expect more children would attain satisfactory sedation prior to anaesthetic induction when higher dose is used.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Patient Between 1-8 Years Old Undergoing Elective Surgery at Queen Mary Hospital

NCT number NCT01065701
Study type Interventional
Source The University of Hong Kong
Contact
Status Completed
Phase Phase 3
Start date July 2009
Completion date August 2010