The effect of propolis supplementation in treatment of non-alcoholic fatty liver

Phase 3

Recruiting

• Conditions: on-alcoholic fatty live.; Fatty (change of) liver, not elsewhere classified; K76.0

• Registration Number: IRCT20100209003320N20
• Lead Sponsor: Tabriz University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 12 July 2021

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 46

Inclusion Criteria

NAFLD (Grade 1 and 2)
Age 20-50 years
Body mass index(BMI) in the range of 30-40 Kg / m2
Willingness to participate in the study

Exclusion Criteria

Pregnancy, lactation and menopause in women
Smoking and alcohol use
Skin or gastrointestinal allergies to propolis, honey and any of the beehive products
Adherence to a special diet three months before the study
Consumption of chemical or herbal medicines for weight loss
Taking antibiotics or various supplements that affect the levels of liver enzymes
Performing weight loss surgery in the last year or strict weight loss diets in the last three months
Suffering from any conditions affecting liver function
Use of hepatotoxic medications
Taking multivitamins or antioxidant supplements during the last 3 months

Study & Design

• Study Type: interventional
• Study Design: Not specified