Healthy volunteers
Conditions
Interventions
Subjects in this group receive 30 mg of nadolol orally with 300 mL of water after overnight fasting. In the second phase, subjects receive 30 mg of nadolol orally with 50 mg of green tea extract diss
Sponsors
Fukushima Medical University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Healthy volunteers
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 ContactOsamu Abe
Fukushima Medical University, School of Medicine Department of Phamacology
Outcome results
None listed