nonalcoholic fatty liver disease fatty liver
Conditions
Interventions
soluble dietary fibrer
D065626
Sponsors
Yoneda Masato
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: nonalcoholic fatty liver disease diagnosised by Evidence-based clinical practice guidelines for nonalcoholic fatty liver disease/nonalcoholic steatohepatitis 2020 and MRI-PDFF more than 3.5%
Exclusion criteria
Exclusion criteria: pregnant pateints, patients who is blest-feeding, patients who can't undergo MRI, patients allergic to this supplements
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Serum ALT levels before and after the end of treatment (12 weeks later) (6 g/day group, 18 g/day group) | — |
Secondary
| Measure | Time frame |
|---|---|
| Serum AST before and after treatment (6 g/day group, 18 g/day group) before and after completion of treatment (12 weeks) Serum gamma-GTP before and after treatment (6 g/day group, 18 g/day group) at the end of treatment (after 12 weeks) MRI-PDFF values before and after treatment (6 g/day group and 18 g/day group) before and after the end of treatment (12 weeks) Change in stool characteristics before and after administration (6 g/day group, 18 g/day group) Comparison of ALT, AST, gamma-GTP, MRI-PDFF and stool characteristics change in different doses of SunFiber (6g/day group vs. 18g/day group) | — |
Contacts
Public ContactMasato Yoneda
Yokohama City University Hospital
Outcome results
None listed