Healthy volunteers
Conditions
Interventions
In the first phase, group 1 subjects receive nadolol orally with water (150 mL) one hour after taking 150 mL of water. In the second phase, the subjects receive nadolol orally with brewed green tea
Sponsors
Fukushima Medical University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Healthy adults
Exclusion criteria
Exclusion criteria: Smoker
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Blood samples are collected before and at 0.5, 1, 2, 3, 4, 6, 8, 24,and 48 hours after nadolol administration. Urine samples are obtained over 48 hours after nadolol administration. Blood pressure and pulse rate are monitored before and at 0.5, 1, 2, 3, 4, 6, 8, 24, and 48 hours after nadolol adoministration. | — |
Secondary
| Measure | Time frame |
|---|---|
| Plasma concentrations of nadolol Urinary excretions of nadolol Blood pressure Pulse rate | — |
Countries
Japan
Contacts
Public ContactShingen Misaka
Fukushima Medical University, School of Medicine Department of Phamacology
Outcome results
None listed