Non-alcoholic fatty liver disease. Fatty (change of) liver, not elsewhere classified
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Willingness to participate in the study people aged 18 to 60 years no history of alcohol consumption no other liver disorders, malignancies, cardiovascular, respiratory and kidney disorders no history of weight loss or bariatric surgery in recent years no drug use In the last 3 months the absence of endocrine and metabolic disorders
Exclusion criteria
Exclusion criteria: Pregnancy or breastfeeding in women The patient's unwillingness to continue participating in the study Non-compliance with the supplement Participating in a concurrent trial Allergy to supplements
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Biochemical markers. Timepoint: 8 weeks. Method of measurement: Colorimetric method.;Oxidative stress. Timepoint: 8 weeks. Method of measurement: Colorimetric method.;Inflammatory cytokine. Timepoint: 8 weeks. Method of measurement: ELISA. | — |
Secondary
| Measure | Time frame |
|---|---|
| Creatinine level. Timepoint: 8 weeks. Method of measurement: colorimetric. | — |
Countries
Iran (Islamic Republic of)
Contacts
Yasouj University of Medical Sciences