MedPath

The effect of propolis supplementation with weight loss diet in treatment of non-alcoholic fatty liver

Phase 2
Recruiting
Conditions
non-alcoholic fatty liver.
Fatty (change of) liver, not elsewhere classified
K76.0
Registration Number
IRCT20100209003320N21
Lead Sponsor
Tabriz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
46
Inclusion Criteria

Both sexes
Age 20-50 years
Body mass index (BMI) in the range of 30-40 Kg/m2
Willingness to participate in the study
Non-alcoholic fatty liver disease (NAFLD) (grades 1 and 2)

Exclusion Criteria

pregnancy, lactation and menopause in women
Skin or gastrointestinal allergies to propolis, honey and any bee products
Smoking or alcohol use
Following a particular diet in the last three months
Using synthetic or herbal medicines for weight loss in the last three months
Performing weight loss surgery in the past year or strict weight loss diets in the last three months
Use antibiotics or supplements affecting liver enzyme levels in the last three months
Having symptoms of infectious or inflammatory disease or recent surgery

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
© Copyright 2025. All Rights Reserved by MedPath