Healthy subjects with serum triglyceride levels in the borderline range
Conditions
Interventions
Specifics of the intervention act (4 tablets/day of tabletized powder, administration period of 30 days) Criteria for implementation of the intervention
ingestion after breakfast Criteria for modification of the intervention
discontinuation of the intervention if any discomfort (diarrhea or other gastrointestinal symptoms, mood disorder, allergic symptoms, etc.) occurs due to ingestion Criteria for discontinuation or com
discontinuation if any intake-related discomfort (diarrhea or other gastrointestinal symptoms, dysphoria, allergic symptoms, etc.) occurs
Specifics of the intervention act (4 tablets/day of tabletized
discontinuation if any intake-related discomfort (diarrhea or other gastrointestinal symptoms, dysphoria, allergic symptoms, etc.) occurs
Sponsors
Tokushima University Graduate School
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: People with triglyceride levels in the 120-149 mg/dL range
Exclusion criteria
Exclusion criteria: Persons with diseases of the liver, kidney, heart, etc. Those who are taking medication for the purpose of treatment of diseases such as lifestyle-related diseases Those who have taken supplements within 1 month of the start of the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Serum triglyceride level | — |
Secondary
| Measure | Time frame |
|---|---|
| Body Fat Percentage body weight | — |
Countries
Japan
Contacts
Public ContactHirohshi Sakaue
Tokushima University Graduate Schoo Institute of Biomedical sciences
Outcome results
None listed