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The effect of chitosan supplementation in patients with nonalcoholic fatty liver disease (NAFLD)

Not Applicable
Conditions
onalcoholic fatty liver.
Nonalcoholic fatty liver disease [NAFLD]
Registration Number
IRCT20180412039284N1
Lead Sponsor
Ahvaz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
50
Inclusion Criteria

Individuals of both genders (males and females) will be selected to participate in the study, aged between 18 and 65 years old that their fatty liver diagnosed by ultrasound testing
No allergies to seafood

Exclusion Criteria

Hepatitis, liver cirrhosis, Wilson's disease, acute fatty liver, pregnancy, hepatocellular carcinoma, hypothyroidism and chronic liver disease
Lipodystrophy
Menopause
Parenteral nutrition
Diseases that involve bile ducts and bile ducts
Severe weight loss (more than 10% of body weight) during last 6 months and weight loss surgery
Congenital metabolic diseases
Consumption of Herbal Supplements in the last three months
Taking drugs that cause fatty liver and liver toxicity (amiodarone, antivirals, spirin, non-steroidal anti-inflammatory drugs, corticosteroids, methotrexate, tamoxifen, tetracycline, valproic acid
Pregnancy and lactation
Consumption of Omega 3 and Vitamin E and other antioxidant supplements over the past 6 months
History of cardiovascular disease and kidney disease
BMI between 25 and 40
Unwillingness to participate
Energy consumption less than 800 or more than 4200kcal/day

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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