None listed
Conditions
Interventions
Dietary Supplement : Consumption of placebo or extract of Dolichos lablab Linne(500mg/d) once a day for 12 weeks.
Sponsors
NovaKmed
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1) Subject who voluntarily agrees to participate and signs in informed consent form 2) Age: = 20 years 3) Subject who has fatty liver 4) one or more of ALT, AST, GGT : = the upper limit of normal levels(ULN) and < ULN?3
Exclusion criteria
Exclusion criteria: 1) Subjects with High quality of the meal (recommended food score > 36) 2) Subjects who constantly performed severe exercises at least 10 hours per week 4) Chronic smoker (= 20 cigarettes/d) 4) alcoholics or Subjects who usually drink alcohol as follows -male = 210 g / week (3.5 bottles of soju/week, 4 glasses/day) -female = 140 g / week (2.5 bottles of soju/week, 3 glasses/day) 5) Continuous consumption of beans or bean products(tofu, soy milk, etc.) within 2 weeks before the first visit 6) Subject with following diseases and past medical history ? diseases related hepatic function -viral hepatitis -serious liver disease(hepatic insufficiency, etc.) primary biliary cirrhosis, drug-induced liver disease -autoimmune liver disease -liver disease induced by drug or operation -inherited liver disease ? infectious disease (tuberculosis, etc.), serious cardiovascular disease, disease of digestive system, renal disease, thyroid disease, autoimmune disease, malignant tumor, multisystem failure, Inflammatory Bowel Disease, serious mental illness,HIV positive 7) Received organ transplantation or bone marrow transplantation 8) Predicted to use prohibited drugs 9) Administration of drugs that affect liver function within 12 weeks before the first visit (medication for hyperlipidemia,antidiabetics, high dose of estrogen or administration of steroid over 14 days 10) Continuous consumption of dietary supplements or oriental medicine within 4 weeks before the first visit 11) Subjects with hypersensitivity to test materials 12) Participation in other human study within 12 weeks before the first visit 13) Pregnant or lactating women 14) Any condition that the principal investigator believes may put the subjects at undue risk
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Hepatic function | — |
Secondary
| Measure | Time frame |
|---|---|
| Hepatic function related markers | — |
Countries
Korea, Republic of
Contacts
Public ContactHyejin Jeong
BiofoodCRO
Outcome results
None listed