Evaluation of the Bioavailability of Dexamethasone in Healthy Subjects

NACompletedINTERVENTIONAL
Enrollment

8

Participants

Timeline

Start Date

November 5, 2021

Primary Completion Date

November 6, 2021

Study Completion Date

November 13, 2021

Conditions
Dexamethasone AdministrationIntranasal AdministrationInflammationIntravenous Drug UsageHealthy Subjects
Interventions
DRUG

Dexamethasone

The nominal doses were similar, volunteers were randomly assigned to receive a single dose of DXM by IV bolus of 1.5 mL (equivalent to 6 mg of dexamethasone) or the same dose intranasally by using a Mucosal Atomization Device (MAD Nasal). allowing direct pharmacokinetic comparison without dose normalization. Venous blood samples were obtained via an indwelling catheter before administration and at 0.25, 0.5, 0.75, 1, 1.5, 2, 3, 4, 8, 12 and 24 h for DXM. Plasma was separated and frozen at -70 °C for further analysis.

Trial Locations (1)

04510

Universidad Nacional Autonoma de Mexico, Mexico City

All Listed Sponsors
lead

Universidad Nacional Autonoma de Mexico

OTHER

NCT05647408 - Evaluation of the Bioavailability of Dexamethasone in Healthy Subjects | Biotech Hunter | Biotech Hunter