Nonalcoholic fatty liver disease
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Meet the diagnostic criteria of NAFLD in Western medicine; 2. Aged 18 to 80 years; 3. Gender is not limited; 4. Subjects agreed to join this clinical study, signed an informed consent voluntarily, and agreed to participate in visits, examinations, and treatment in accordance with the requirements of the research program.
Exclusion criteria
Exclusion criteria: 1. Pregnant and lactating women; 2. Patients considered unsuitable by the investigator to participate in this study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Proportion of patients whose ALT level returned to normal (= 30% after treatment;Changes of computed tomography liver spleen ratio before and after treatment;Changes of total cholesterol (TC) ratio before and after treatment and the proportion of patients who returned to normal (<= 5.17 mmol / L) after treatment;Changes of Traditional Chinese Medicine syndrome score before and after treatment; | — |
Secondary
| Measure | Time frame |
|---|---|
| Changes of liver function before and after treatment ;Changes in glucose and lipid metabolism before and after treatment;Body Mass Index;Changes of liver imaging before and after treatment; | — |
Countries
China
Contacts
Longhua Hospital Affiliated to Shanghai University of traditional Chinese Medicine; Xinhua Hospital Affiliated to Medical College of Shanghai Jiaotong University