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Evaluation of the effects of a low free sugar diet in patients with Nonalcoholic fatty liver disease

Evaluation of the effects of a low free sugar diet on lipid profile, glycemic indices, liver enzymes, inflammatory factors and hepatic steatosis and fibrosis in patients with Nonalcoholic fatty liver disease

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20100524004010N30
Enrollment
42
Registered
2020-06-11
Start date
2019-07-23
Completion date
Unknown
Last updated
2020-06-15

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

Conditions

Nonalcoholic fatty liver disease. low free sugar diet, lipid profile, glycemic indices, liver enzymes, inflammatory factors, hepatic steatosis , fibrosis , patients with Nonalcoholic fatty liver disease

Interventions

Intervention 1: Intervention group: a low free sugar diet with dietary and physical activity recommendations/12 weeks. Intervention 2: Control group: Dietary and physical activity recommendations/12 w

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: The desire to participate in research Age 60-18 years BMI above 20 Evidence of non-alcoholic steatohepatitis (inflammation and swelling of hepatocytes) second and third degree in ultrasonography Evidence of non-alcoholic steatohepatitis in fibro-scan results with CAP Score over 263 Lack of a history of alcohol consumption or alcohol consumption less than 10 grams per day in women and less than 20 grams per day in men Lack of other chronic and acute liver diseases and disorders (hepatitis B, C, etc.), biliary disease, autoimmune diseases, cancer and hereditary disorders affecting the condition of the liver (iron, copper storage disease) and cirrhosis Lack of pregnancy or lactation in women No consumption of hepatotoxic drugs such as phenytoin, tamoxifen and lithium, and drugs that affect liver function

Exclusion criteria

Exclusion criteria: Lack of desire to continue research Forced to use antibiotics or hepatotoxic drugs during the study Non-compliance with low free sugar diet

Design outcomes

Primary

MeasureTime frame
Hepatic steatosis, Liver fibrosis. Timepoint: At the first and at the 12th week of the study. Method of measurement: Fibroscan.

Secondary

MeasureTime frame
Weight. Timepoint: At the first , 6th and 12th week of the study. Method of measurement: Scale.;BMI. Timepoint: At the first , 6th and 12th week of the study. Method of measurement: Calculate.;Waist to hip ratio. Timepoint: At the first , 6th and 12th week of the study. Method of measurement: Calculate.;Liver enzymes (AST,ALT,GGT). Timepoint: At the first and at the 12th week of the study. Method of measurement: Enzymatic method.;Lipid profile (TG,Total cholesterol,LDL-C,HDL-C). Timepoint: At the first and at the 12th week of the study. Method of measurement: Enzymatic method.;FBS. Timepoint: At the first and at the 12th week of the study. Method of measurement: Enzymatic method.;Insulin. Timepoint: At the first and at the 12th week of the study. Method of measurement: Radioimmunoassay.;Hs-CRP. Timepoint: At the first and at the 12th week of the study. Method of measurement: ELISA.;TNF-a. Timepoint: At the first and at the 12th week of the study. Method of measurement: ELISA.;NF-?B. Timepoint: At the first and at the 12th week of the study. Method of measurement: ELISA.;HOMA-IR. Timepoint: At the first and at the 12th week of the study. Method of measurement: Calculate.;QUICKI. Timepoint: At the first and at the 12th week of the study. Method of measurement: Calculate.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactazita hekmatdoost

Shahid Beheshti University of Medical Sciences

a_hekmat2000@yahoo.com+98 21 2235 7483

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026