Safety evaluation of long term intake of test supplement
- Conditions
- Healthy subjects
- Registration Number
- JPRN-UMIN000044208
- Lead Sponsor
- FANCL Corporation
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 60
Not provided
1. Subjects who are judged as unsuitable for the study based on the results of clinical laboratory test or cardiopulmonary function. 2. Subjects who have allergy related to this study. 3. Subjects who have diseases requiring continuous medication, or serious medical history who needed medication. 4. Subjects whose clinical laboratory tests, blood pressure, and physical measurements before intake of trial supplements are significantly out of the standard values. 5. Subjects who have participated in other clinical studies. 6. Females who are known or suspected to be pregnant, breastfeeding or desire to become pregnant during the trial period. 7. Subjects who are judged as unsuitable for the study based on the answers of background survey. 8. Subjects who are 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 Hematologic test Blood biochemistry test Urine analysis Blood pressure/pulsation Body weight/body mass index Doctor's question Adverse event
- Secondary Outcome Measures
Name Time Method