Dexmedetomidine Clinical Trial
Official title:
Crossover Pharmacokinetic Study of Two Mode of Administration of Intranasal Dexmedetomidine in Healthy Adult Volunteers
Intranasal dexmedetomidine has been studied and used in children for premedication before
anaesthesia or fro sedation. It can be administered by simple dripping or by Mucosal
Atomization Device (MAD®).
Since MAD® delivers intranasal medication in a fine mist, it is possible that absorption and
bioavailability would be better compares to simple dripping method. To date no
pharmacokinetic information of intranasal dexmedetomidine delivered by either method is
available. This investigation is designed to compare the bioavailablity of intranasal
dexmedetomidine deliver via simple dipping with tuberculine syringe and MAD® in healthy
adults.
This is a three-period crossover double-blinded study. 8 subjects will be recruited and they will attend 3 study sessions after informed written and verbal consent. They would have dexmedetomidine administered via different rout each time, intravenous, intranasal via dripping or intranasal via atomizer. Blood samples are collect to determine bioavailability of each mode of drug delivery. ;
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