Measurement of plasma concentrations of yokukansan in form of suppository to healthy Japanese volunteers
Not Applicable
- Conditions
- healthy Japanese volunteers
- Registration Number
- JPRN-UMIN000012965
- Lead Sponsor
- issay Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up continuing
- Sex
- All
- Target Recruitment
- 5
Inclusion Criteria
Not provided
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.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time course of plasma levels of hirsuteine and geissoschizine methylether after enteric administration of yokukansan
- Secondary Outcome Measures
Name Time Method Time course of plasma levels of hirsuteine and geissoschizine methylether after oral administration of yokukansan