Nonalcoholic fatty liver disease/Nonalcoholic steatohepatitis
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients diagnosed as NAFLD/NASH
Exclusion criteria
Exclusion criteria: 1.Women with pregnancy or possible pregnancy 2.Patients with severe renal failure and heart failure 3.Patient who is considered to be inappropriate for entry into the trial by the investigator 4.Medical doctors decided the patients are inappropriate. 5.Patients with substantial alcohol consumption (20g/day for women or >30g/day for men). 6.Patients with poor glycemic control (HbA1c>9.0%) 7.Patients with other active hepatitis and hepatocellular carcinoma 8.Patients with history of gastrointestinal surgery 9.Patients who take nonabsorbable antibiotic
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Improvement of liver enzyme | — |
Secondary
| Measure | Time frame |
|---|---|
| 1.Changes of short-chain fatty acid (Butyric acid,Acetic acid,Propionic acid etc.) 2.Changes of pathologic and metabolic marker (HOMA-IR, NAFIC socre, NAFLD fibrosis sore, FIB-4 index, APRI index, T.Cho, LDL-Cho, HDL-Cho, TG, FFA, ferritin, fasting glucose,HbA1c, high sensitivity CRP etc.) 3.Changes of hepatic fibrosis markers 4.Changes of degree of fatty liver by abdominal ultrasound examination 5.Correlation of gut microbiota and therapeutic effect 6.Changes of body weight and BMI 7.Metabolome and protein analysis of metabolite in feces 8.Changes of bile acid 9.Correlation between expiratory noble gases, gut microbiota and NAFLD/NASH 10.Correlation between usefulness of kestose and disease prognosis in the patients with NAFLD/NASH | — |
Countries
Japan
Contacts
Nagoya University Hospital Department of Gastroenterology and Hepatology