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Lifestyle Changes in Fatty Liver; Additive Effect of Honey Intake

Lifestyle Changes in Fatty Liver; Additive Effect of Honey Intake

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06596109
Enrollment
40
Registered
2024-09-19
Start date
2024-09-10
Completion date
2025-02-15
Last updated
2024-09-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Fatty Liver, Nonalcoholic

Brief summary

honey is a natural functional food used in control cardiovascular risk factors but its effect on fatty liver is not investigated

Detailed description

Forty fatty liver (non-alcoholic from) patients with obesity are included to be divided into group 1 who will contain 20 patients who will receive honey intake (orally, as a daily total dose of 2 g/kg, this dose will be divided to three equal subdoses, every dose will be administered before meal), low calorie diet, and treadmill walking (40 minutes per session, three times per week) for 12 weeks. Group 2 who will contain 20 patients who will receive low calorie diet, and treadmill walking (40 minutes per session, three times per week) for 12 weeks.

Interventions

BEHAVIORALhoney intake and lifestyle changes

Twenty fatty liver (non-alcoholic from) patients with obesity are included as 20 patients who will receive natural unprocessed honey intake (orally, as a daily total dose of 2 g/kg, this dose will be divided to three equal subdoses, every dose will be administered before meal), low calorie diet, and treadmill walking (40 minutes per session, three times per week) for 12 weeks.

Twenty fatty liver (non-alcoholic from) patients with obesity are included as 20 patients who will receive low calorie diet and treadmill walking (40 minutes per session, three times per week) for 12 weeks.

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
30 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

* fatty liver (non alcoholic form) * both sexes included * obese subjects (class I)

Exclusion criteria

* cardiac insult * respiratory insult * renal insult * lower limb insult

Design outcomes

Primary

MeasureTime frameDescription
High density lipoproteinit will be assessed after 12 weeksit will be measured in serum

Secondary

MeasureTime frameDescription
cholesterolit will be assessed after 12 weeksit will be measured in serum
low density lipoproteinit will be assessed after 12 weeksit will be measured in serum
alanine transamianseit will be assessed after 12 weeksit will be measured in serum
triglyceridesit will be assessed after 12 weeksit will be measured in serum
fasting blood glucoseit will be measured after 12 weeksit will be measured in serum
body mass indexit will be measured after 12 weeksit will be measured on empty stomach
waist circumferenceit will be measured after 12 weeksit will be measured on empty stomach
aspartate transamianseit will be assessed after 12 weeksit will be measured in serum

Countries

Egypt

Contacts

Primary ContactAli MA Isamil, Lecturer
ali.mohamed@pt.cu.edu.eg0201005154209
Backup ContactAlshaymaa S Abd El-Azeim, Lecturer
Shimaashaaban30@yahoo.com021033771553

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026