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Completed

NCT Number: NCT07304336

Dietary Strategies for MASLD (Metabolic Dysfunction-Associated Steatotic Liver Disease)

This is a non-blinded, three-arm, parallel, 6-month randomized, longitudinal, and controlled intervention trial. designed to compare the effects of three dietary regimes (Mediterranean diet, low-carbohydrate diet and standard nutritional recommendations) on non-invasive parameters of fat accumulation and liver damage, including radiological and biochemical tests, in overweight or obese subjects with MASLD. Participants were enrollment and screening from the Liver Unit of the Department of Medical Sciences, University of Torino and randomly assigned to one of three groups: a low-carbohydrate diet, a mediterranean diet, or standard nutritional recommendations.

All participants were submitted to the following assessments both at enrollment and at after 6 month at the end of the study: 3-day food record; the Medi-Lite score; anthropometric measurements (weight, height, BMI, waist and neck circumferences); fat mass, fat-free mass by bioelectrical impedance; hand-grip strength; energy expenditure by indirect calorimetry; blood pressure measurement; blood sampling for metabolic variables and biomarkers of liver damage and liver disease measures (Cap, Stiffness and Fib-4).

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

AOU Città della Salute e della Scienza di Torino, University of Torino, Torino.

Torino, 10126, Italy

About this study

This is a three-arm, parallel-group, open-label randomized controlled trial designed to evaluate the effectiveness of three different nutritional interventions on non-invasive markers of liver damage, including radiological and biochemical assessments. Patients with MASLD were recruited from the Liver Unit of the Department of Medical Sciences, University of Torino.

At baseline, participants were randomly assigned to one of the following three groups:

A) Low-carb Diet (LCHO: 35-40% carbohydrates, 30% protein, 30-35% fats.) B) Mediterranean Diet (MeD: 50-60% carbohydrates, 15% protein, 25-35% fats ) C) Control group: standard nutritional recommendations The following evaluations were performed both at baseline and after 6 months at the and of the study: 3-day food record; the Medi-Lite score; anthropometric measurements (weight, height, BMI, waist and neck circumferences, fat mass, fat-free mass by bioelectrical impedance); hand-grip strength; energy expenditure by indirect calorimetry; blood pressure measurement; blood sampling for metabolic variables and biomarkers of liver damage and liver disease measures (Cap, Stiffness and Fib-4).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • age ≥18 and <75 years
  • BMI ≥25 and <35 kg/m2
  • not having previously received nutritional advice for the liver disease

Exclusion criteria

  • other causes of liver disease (including viral, autoimmune, cholestatic, genetic, alcoholic, and drug-induced)
  • other diseases or conditions requiring specific dietary recommendations
  • a history of alcohol abuse
  • diabetes mellitus
  • pharmacological treatments potentially interfering with study outcomes (corticosteroids, glucagon-like-peptide 1 agonists, biologic drugs)
  • pregnancy or breastfeeding
  • inability to give written informed consent
  • life expectancy expected to be <1 year.

Treatment and study plan

Low-Carb diet

Behavioral

Participants followed a low-carbohydrate diet for 6 months. Macronutrient distribution: 35-40% carbohydrates, 30% protein, 30-35% fats. The diet was tailored based on participants' energy requirements.

Mediterranean Diet

Behavioral

Participants followed a Mediterranean-style diet for 6 months, providing 50-60% of energy from carbohydrates, approximately 15% from protein, and 25-35% from fat. The diet was tailored to individual energy requirements and patients in this group, should consume moderate portions of fish, poultry, and dairy products. The recommended cereal servings were larger than those for the LCHO arm.

Standard Lifestyle Recommendations

Behavioral

Participants received standard nutritional raccomandations for 6 months, including guidance on healthy eating, advices for regular physical activity, and educational materials consistent with standard clinical practice. No specific dietary plan was prescribed.

Primary outcomes

  1. Within- and between-group changes in hepatic steatosis [percentage, %]

    Time frame: 6 months

    The unit of measure is the percentage (%) of liver fat content, as assessed by transient elastography - FibroScan®.

  2. Within- and between-group changes in Controlled Attenuation Parameter. (CAP) [dB/m]

    Time frame: 6 months

    The unit of measure is decibels per meter (dB/m), as measured by transient elastography - FibroScan®.

Secondary outcomes

  1. Change in liver stiffness measured by transient elastography - FibroScan®. [kilopascals, kPa]

    Time frame: 6 months

    Liver stiffness will be assessed using transient elastography - FibroScan®.

  2. Changes in fibrosis-4 index

    Time frame: 6 months

    Within- and between-group changes in fibrosis-4 index, a non-invasive score for liver fibrosis calculated by the following formula:

    FIB-4= (age x AST / (platelet count (x 10 9 ) x√ALT). This index has no fixed upper limit; higher values indicate worse fibrosis.

  3. Changes in fat mass percentage

    Time frame: 6 months

    Within- and between-groups changes in fat mass percentage measured by bioelectrical impedance analysis

  4. Changes in energy expenditure.

    Time frame: 6 months

    Within- and between-group changes in energy expenditure measured by indirect calorimetry.

  5. Changes in insulin restistance [mmol/LxμU/mL]

    Time frame: 6 months

    Within- and between-group changes in HOMA-IR [mmol/LxμU/mL]

  6. Changes in serum transaminase levels

    Time frame: 6 months

    Within- and between-group changes in serum transaminase levels [U/L]

  7. Changes in thrombospondin-2 (TSP2) [ng/ml]

    Time frame: 6 months

    Assessing serum Thrombospondin-2 (TSP2) changes across incremental delta of weight loss

  8. Changes in C-terminal procollagen 4 (PRO-C4) [ng/ml]

    Time frame: 6 months

    Assessing serum C-terminal procollagen 4 (PRO-C4) changes across incremental delta of weight loss

Sponsors and collaborators

Lead sponsor

University of Turin, Italy

Other

Registry information

Official study title

Comparing the Efficacy of Dietary Strategies in Managing Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD): a Randomized Controlled Trial

Important dates

Study start
2022
Primary completion
2025
Study completion
2025
First posted
Dec 26, 2025
Registry last updated
Jan 12, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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