healthy Japanese volunteers
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: a) Healthy volunteers b) Agreement to sign an informed consent
Exclusion criteria
Exclusion criteria: a) Patients who are allergic to medicines, or foods related to the test material of this trial b) Pregnant women, lactating women, or women who want to get pregnant during the trial period c) Patients who are enrolled in the other clinical trials before the agreement for the participation to this trial d) Patients who are judged not suitable to participate in this trial by physician.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Time course of plasma levels of hirsuteine and geissoschizine methylether after enteric administration of yokukansan | — |
Secondary
| Measure | Time frame |
|---|---|
| Time course of plasma levels of hirsuteine and geissoschizine methylether after oral administration of yokukansan | — |
Countries
Japan
Contacts
Nissay Hospital Anesthesiology and Palliative care