metabolic dysfunction-associated fatty liver disease
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: (1) patients with the diagnostic criteria of MAFLD (2) patients at age 18-65; (3) individuals with body mass index (BMI) between 18.5 and 35; (4) Volunteer to participate in the study and sign the informed consent
Exclusion criteria
Exclusion criteria: (1) Patients who have progressed to the decompensated stage of cirrhosis; (2) Women in the pregnancy or breastfeeding period, allergic people; (3) Patients with other serious brain, heart, lung, kidney, blood system, connective tissue and muscle system, malignant tumor diseases and mental diseases in addition to hypertension, diabetes, hyperlipidemia; (4) Patients with severe metabolic disorders, including uncontrolled hypertension (diastolic blood pressure =100 mmHg or systolic blood pressure =180 mmHg), type I diabetes mellitus, type II diabetes mellitus with brain, eye, kidney complications, type II diabetes mellitus with poor blood glucose control and HBA1c > 10%; (5) People who have used any other drug within 3 months that affects liver function, causes hepatic steatosis, or may have an impact on this study (including tamoxifen, ethamiodarone, sodium valproate, methotrexate, glucocorticoids, probiotics, amiodarone, olazepine).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| HFC;liver function;Blood lipid;Weight change; | — |
Secondary
| Measure | Time frame |
|---|---|
| Waist circumference;blood sugar;blood pressure;hs-CRP;Oxidative stress indicators; | — |
Countries
CHINA
Contacts
Department of Gastroenterology, China-Japan Friendship Hospital, Beijing, China