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vitamin D and non-alcoholic fatty liver disease

Not Applicable
Conditions
on-alcoholic fatty liver disease.
Fatty (change of) liver, not elsewhere classified
Registration Number
IRCT201503163320N10
Lead Sponsor
Vice Chancellor for research of Tabriz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
72
Inclusion Criteria

willingness to participate in the study, 18-50 years old, liver steatosis on sonographic image, vitamin D deficiency(25(OH)D levels less than 30ng/ml), BMI=25
Exclusion criteria: Alcohol consumption(more than 20g/day), menopause, gestation or lactation, BMI>40, diabetes and insulin resistance, any other liver disease(viral disease, Wilson, Hemochromatosis, glycogen storage disorders and etc) or using drugs for the treatment of fatty liver(such as omega-3 and herbal supplements), Thyroid and parathyroid disorders, bone problems, Cushing's syndrome, fat malabsorption, cholecystectomy and any other disease that affect the liver, renal disease(renal failure and nephrolithiasis), using vitamin D, calcium and vitamin E supplements in the past 6 months, taking any drugs causing fatty liver or hepatotoxic drugs(calcium channel blocker,methotrexate,tamoxifen, valproate, diltiazem, amiodarone, isoniazid, corticosteroids and high-dose of estrogen and progestin, and the use of contraceptives), taking drugs affecting insulin resistance and liver function(Such as metformin, pioglitazone, lovastatin and etc.), get weight loss diet in the past 6 months, using total parenteral nutrition in the past 6 months.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Serum 25(OH)D. Timepoint: Beginning and end of the intervention. Method of measurement: ELIZA.;Serum Adiponectin. Timepoint: Beginning and end of the intervention. Method of measurement: ELIZA.;Liver Enzyme (ALT,AST,ALP). Timepoint: Beginning and end of the intervention. Method of measurement: IFCC.;Liver steatosis. Timepoint: Beginning and end of the intervention. Method of measurement: Liver Sonography.
Secondary Outcome Measures
NameTimeMethod
Anthropometry. Timepoint: Begining and end of intervention. Method of measurement: Scale and meter and bioelectrical impedance analyzer.;Energy and nutrient intake. Timepoint: Beginning and end of the intervention. Method of measurement: 24- hour dietary recall.;Physical activity. Timepoint: Begining and end of intervention. Method of measurement: Physical activity Questionnaire.;Sun exposure. Timepoint: Begining and end of intervention. Method of measurement: Questionnaire.
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