Healthy volunteers
Conditions
Interventions
Subjects receive an oral dose of lisinopril (Zestril 10mg tablet, Astrazeneca) with 200 ml of water after overnight fasting. Blood sampling and measurements of pulse rate and blood pressure are perfor
Sponsors
Fukushima Medical University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: To be healthy without receiving medicines regularly
Exclusion criteria
Exclusion criteria: Smoker
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Area under the plasma concentration-time curve (AUC) of lisinopril | — |
Secondary
| Measure | Time frame |
|---|---|
| Urinary excretion of lisinopril | — |
Countries
Japan
Contacts
Public ContactShingen Misaka
Fukushima Medical University Department of Pharmacology
Outcome results
None listed