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Effect of probiotics on patients with NAFLD

Not Applicable
Conditions
on Alchoholic Fatty Liver Disease.
Fatty (change of) liver, not elsewhere classified
Registration Number
IRCT2012122911920N1
Lead Sponsor
Baqiyatallah University of Medical Science
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
60
Inclusion Criteria

patients with NAFLD; the age range was 18 to 65 years old.
Exclusion criteria: patients with NAFLD that used supplemental probiotics of probiotic foods during last 3 monthes; also those used tobacco and alcohol; patients with cardiovascular diseases, chronic liver and kidney diseases, Wilson disease, Hemochromatosis; people with low immune system ability (autoimmune) and pregnant or lactating women.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Malodialdehyde (MDA). Timepoint: Before and after Intervention. Method of measurement: ELISA.;TAC. Timepoint: Before and after Intervention. Method of measurement: ELISA.;Serum Insulin Levels. Timepoint: Before and After Intervention. Method of measurement: ELISA.;IL-6. Timepoint: Before and After Intervention. Method of measurement: ELISA.;Serum Glucose. Timepoint: Before and after Intervention. Method of measurement: Autoanalyzer.;Lipid Profile ( Tg,Total Chol, LDL-C, HDL-C ). Timepoint: Before and After Intervention. Method of measurement: Autoanalyzer.;TNF-a. Timepoint: Before and after Intervention. Method of measurement: ELISA.;OxLDL. Timepoint: Before and after Intervention. Method of measurement: ELISA.;ALT. Timepoint: Before and after Intervention. Method of measurement: autoanalyzer.;AST. Timepoint: Before and after Intervention. Method of measurement: autoanalyzer.
Secondary Outcome Measures
NameTimeMethod
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