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Effect of probiotics in Nonalcoholic Fatty Liver

Phase 3
Recruiting
Conditions
K76.0
onalcoholic Fatty Liver.
Fatty (change of) liver, not elsewhere classified
Registration Number
IRCT20231229060558N1
Lead Sponsor
Mashhad University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
120
Inclusion Criteria

People between 20 and 75 years old with confirmed fatty liver in Persian Cohort of Mashhad

Exclusion Criteria

•Liver failure
• Suffering from hepatitis (viral, autoimmune, metabolic, medicinal)
• History of alcohol consumption
• People with ALT or AST more than 5 times normal •
• Pregnant people
•Taking drugs that can cause hepatic steatosis, including antiarrhythmic drugs (Amiodarone) ), anti-metabolite antineoplastic drugs (methotrexate), hormonal antineoplastic drugs (tamoxifen), corticosteroids, anticonvulsant drugs, antiretroviral drugs
• use of antihypertensive drugs, vastatins)
• known hereditary defects (iron and copper). Storage diseases and alpha 1 antitrypsin deficiency

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The percentage of people with non-alcoholic fatty liver disease with a score of at least 2. Timepoint: Examining tests three months after start of using probiotics. Method of measurement: Liver tests including sugar and fat profile, ultrasound of the liver and bile ducts, and fibroscan of the liver.
Secondary Outcome Measures
NameTimeMethod
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