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Evaluation of Oleoylethanolamide supplementation in the prevention and treatment of non-alcoholic fatty liver disease

Phase 3
Conditions
on-alcoholic fatty liver disease.
Fatty (change of) liver, not elsewhere classified
K76.0
Registration Number
IRCT20110530006652N2
Lead Sponsor
Tabriz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
74
Inclusion Criteria

Age between 20 to 50 years old
Body mass index (BMI) of 30 to 40 Kg/m2
Diagnosis of non-alcoholic fatty liver disease by a radiologist based on ultrasonography

Exclusion Criteria

Regular use of non-steroidal anti-inflammatory drugs (NSAIDs), antibiotics and corticosteroids
Use of hormonal drugs, hepatotoxic drugs (such as Phenytoin, Amiodarone, Levothyroxine, Tamoxifene and Lithium), anti-hypertensive drugs, weight loss and lipid lowering drugs
Use of prebiotic and probiotic supplements, vitamins, minerals, antioxidants, and omega 3 supplements
Diagnosed pathological conditions affecting the liver such as liver transplantation, acute or chronic hepatic impairment, viral hepatitis, cystic fibrosis, Haemochromatosis, Wilson's disease, Alpha-1 antitrypsin deficiency, and acute systemic disease
Diagnosed thyroid disorders
Diagnosed kidney diseases
Diagnosed gastrointestinal diseases (e.g. Celiac disease)
Diagnosed diabetes
Diagnosed heart failure
Diagnosed autoimmune diseases
Diagnosed malignancies
Diagnosed severe psychological disorders
Pregnancy and lactation

Study & Design

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