Pharmacokinetic and Metabolic Analysis of Maoto
Not Applicable
- Conditions
- Healthy adult
- Registration Number
- JPRN-UMIN000023609
- Lead Sponsor
- Kochi Medical School
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- Male
- Target Recruitment
- 4
Inclusion Criteria
Not provided
Exclusion Criteria
(1) Allergy (2) Prticipate to other clinical trials within 16 weeks (3) Blood donation more than 400 ml within 12 weeks (4) Severe liver, heart or blood disease (5) Alchol and smooking (6) Drugs (7) Supllyments or diets which contains the ingredients of Maoto (8) Diagnosed as inappropriate by doctor (9) Positive HCV antibody, HBs antigen, and HIV antibody (10) Use of amphetamine and methamphetamine
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Detect of ingredients delivers from Maoto in plasma.
- Secondary Outcome Measures
Name Time Method Calculation of PK parameters and detect of ingredients delivers from Maoto in urine.