Study on blood kinetics of processed plant powder
- Conditions
- Healthy adult
- Registration Number
- JPRN-UMIN000030260
- Lead Sponsor
- HUMA R&D CORP
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 12
Not provided
1)Currently in treatment with medication or seeing a doctor for treatment. 2)Previous history of hepatic disorder, severe kidney, endocrine, cardiovascular, gastrointestinal, pulmonary, hematological, or metabolic disorder, or a complication of these. 3)Pregnant, having the potential to become pregnant, or having anemia. 4)Previous history of drug allergy, food allergy, or any abnormality resulted from ingestion of the study plant. 5)Intake of a prescription drug, an over-the-counter drug, a quasi drug, a food product, a health food product, etc. that contains the study plant or a relative plant within the last month. 6)Extreme faddiness. 7)Extremely irregular lifestyle including irregular meal and sleeping patterns. 8)Presence or previous history of mental disorder (depression, etc.). 9)Participation in any other clinical study involving human subjects within 3 months or current participation in any other clinical study involving human subjects. 10)Regular alcohol consumption with an average of 30g/day or more (500 ml of beer, 180 ml of sake), or alcohol consumption of 30g/day or more (500 ml of beer, 180 ml of sake) for at least four days/week. 11)Smoker. 12)Subjects who are deemed to be unsuitable by the investigator.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Amount of saponin in plasma
- Secondary Outcome Measures
Name Time Method Blood test (hematologic, biochemical tests)