Bioavailability study of lutein from Chlorella
Not Applicable
Completed
- Conditions
- Not Applicable
- Registration Number
- KCT0000750
- Lead Sponsor
- Ewha Womans University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 36
Inclusion Criteria
Voluntarily agree to participate and sign in informed consent form
- Age: 20-50 years
- BMI: 20kg/m2 = ~ < 25kg/m2
Exclusion Criteria
- Subject who takes dietary supplements or medicines that affect eye health or antioxidative capacity within 4 weeks before the first visit.
- Subject who has following diseases: macular degeneration, cataract or any other ophthalmic diseases, hepatic dysfunction, renal dysfunction.
- Subject who participated in another clinical trials within 4 weeks before the first visit.
- Alcoholics
- Smoker
- Subject who is pregnant or breast feeding.
- Subject who has an allergy to the ingredients of study product.
- Any condition that would make the subject unsuitable for enrollment in this study.
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Serum carotenoids concentrations
- Secondary Outcome Measures
Name Time Method Concentration of carotenoids (lutein, zeaxanthin) in buccal mucosa cells