Safety evaluation of excessive intake of supplements containing plant extract
- Conditions
- Healthy adults
- Registration Number
- JPRN-UMIN000052312
- Lead Sponsor
- FANCL Corporation
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 20
Not provided
1. Subjects who are judged as unsuitable for this study by the investigational doctor based on the results of clinical examination or cardiopulmonary abnormality 2. Subjects who may be at risk of developing allergies in relation to the study 3. Subjects who have a disease requiring habitual medication, subjects with a disease under treatment (excluding dry eye and dental caries treatment), and persons with a history of a serious disease requiring medication treatment 4. Subjects whose screening test physical, physical examination and clinical examination values are significantly out of the reference range 5. Subjects who are participating in other clinical studies 6. Subjects who intend to become pregnant or lactating 7. Subjects who are judged as unsuitable for the study based on the results of background survey 8. who are judged to be unsuitable as research subjects (subjects) based on the results of the screening test 9. Subjects Who judged as unsuitable for the study by the investigator for other reasons
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Adverse events, physical measurement (body weight and body mass index), physical examination (blood pressure, heart rate), and laboratory tests (hematology test, blood biochemistry test, urine test)
- Secondary Outcome Measures
Name Time Method