A human study to evaluate tolerance and safety of D-Allulose
Not Applicable
Completed
- Conditions
- Endocrine, nutritional and metabolic diseases
- Registration Number
- KCT0003989
- Lead Sponsor
- Samyang
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
1) Subject who voluntarily agrees to participate and signs in informed consent form
2) Healthy people over 20 years old.
Exclusion Criteria
1) Subject with diseases and past medical history
2) Administration of drugs, dietary supplement, oriental medicine within 4 weeks before the
first visit
3) Subjects with hypersensitivity to test materials
4) Participation in other human study within 4 weeks before the first visit
5) Pregnant or lactating women
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Hematological test(WBC, RBC, Hb et al.);Blood chemical test(ALP, BUN, creatinine et al.);Urine test(pH, protein,glucose et al.)
- Secondary Outcome Measures
Name Time Method Adverse events;Vital signs