The aim of this study is to investigate the safety, pharmacokinetics, pharmacodynamics of intranasal dexmedetomidine, and comparative pharmacokinetics of intranasally and intravenously administered dexmedetomidine in healthy volunteers.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
48
Intranasal Dexmedetomidine
Intravenous Dexmedetomidine
Intranasal Placebo
The Third Xiangya Hospital of Central South University
Changsha, Hunan, China
RECRUITINGAdverse Events
Number of subjects with adverse events
Time frame: Baseline to 7 days after dose administration
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Intravenous Placebo