Skip to main content
OpenTrials
Enrolling by Invitation

NCT Number: NCT06826807

Hepatic Elastography-Enhanced Lifestyle Modification in MASLD

The 2022 National Health Survey in Thailand revealed a substantial rise in obesity and metabolic dysfunction-associated steatotic liver disease (MASLD). The prevalence of MASLD was 19.7%, with higher rates observed in individuals with metabolic syndrome and diabetes. Effective management of MASLD primarily involves lifestyle modifications, including dietary adjustments and increased physical activity. Evidence suggests that patients unaware of their liver fibrosis status are less likely to adhere to these interventions. This study aims to evaluate the impact of hepatic elastography monitoring on lifestyle modification adherence and health outcomes in patients with MASLD over 48 weeks.

Enrolling by Invitation

Interested in participating?

Request Info

Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Faculty of Medicine Siriraj Hospital, Mahidol University

Bangkoknoi, Bangkok, 10700, Thailand

About this study

The 2022 health survey of Thai adults (aged ≥18 years) reported an obesity prevalence of 44.9% (40.3% in males, 49.2% in females), a significant increase over past decades. Obesity is a major contributing factor to the rising incidence of MASLD, previously termed nonalcoholic fatty liver disease (NAFLD). MASLD is defined as fatty liver disease occurring in individuals consuming less than 140 grams of alcohol per week for females or less than 210 grams per week for males, alongside clinical features of metabolic dysfunction.

Among 18,588 surveyed individuals, the prevalence of MASLD was 19.7% (20.9% in males, 18.6% in females), with notably higher rates of 43.5% in those with abdominal obesity and 35.6% in individuals with diabetes. Significant associations were observed between MASLD and factors such as age, sex, physical activity, smoking, and metabolic abnormalities, including overweight, abdominal obesity, elevated triglycerides, diabetes, hypertension, and low HDL cholesterol levels.

MASLD is closely linked to insulin resistance, a critical risk factor for cardiovascular disease. Current guidelines emphasize weight loss through dietary control and exercise to reduce hepatic fat accumulation, inflammation, and fibrosis, while improving metabolic parameters such as blood glucose, lipid profiles, and insulin sensitivity. Behavioral and environmental factors, including high-calorie diets and sedentary lifestyles, contribute to the pathogenesis of MASLD by promoting insulin resistance and hepatic fat accumulation, leading to oxidative stress, inflammation, and fibrosis, thereby increasing the risks of cirrhosis and hepatocellular carcinoma.

A recent study highlighted that 59.2% of MASLD patients were unaware of their liver fat and fibrosis status. Lack of awareness was associated with poor adherence to lifestyle modifications, particularly in obese individuals (BMI > 30 kg/m²). This randomized controlled trial investigates the effect of hepatic elastography monitoring on lifestyle changes, hepatic steatosis, metabolic parameters, and anthropometry, compared to standard care over a 48-week period.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Participants must be diagnosed with MASLD according to the diagnostic criteria outlined in the multi-society Delphi consensus statement on new fatty liver disease nomenclature 2023, with evidence of hepatic steatosis and alcohol consumption of less than 140 grams per week for females or less than 210 grams per week for males, along with at least one clinical characteristic of metabolic syndrome.
  • Participants must be at least 18 years old and less than 80 years old at the time of enrollment.

Exclusion criteria

  • Individuals diagnosed with other chronic liver diseases, including hepatitis B or C, autoimmune hepatitis, Wilson's disease, liver cancer, hemochromatosis, or liver cirrhosis.
  • Individuals diagnosed with conditions that may influence MASLD, such as HIV, chronic inflammatory diseases, or connective tissue disorders.
  • Individuals taking medications known to promote fatty liver disease, such as amiodarone, steroids, methotrexate, hormonal medications, or immunosuppressants.
  • Individuals who have previously taken medications known to impact fatty liver disease, including vitamin E, pioglitazone, GLP-1 receptor agonists, or SGLT2 inhibitors.
  • Participants intending to join weight loss programs or undergo bariatric surgery for obesity treatment.
  • Individuals with severe chronic diseases presenting symptoms during physical activity, such as coronary artery disease, chronic obstructive pulmonary disease, or severe osteoarthritis, which may exacerbate their condition.
  • Patients with contraindications to undergoing MRI examinations, such as claustrophobia or incompatible body implants or materials.
  • Women who are pregnant.
  • Individuals who do not provide formal consent to participate in the research project.

Treatment and study plan

Regular monitoring with transient elastography

Other

MASLD patients were received their liver fat and fibrosis status regularly using transient elastography

Primary outcomes

  1. Change from baseline in non-invasive marker magnetic resonance imaging-estimated proton density fat fraction (MRI-PDFF) (%)

    Time frame: 48 weeks

    Hepatic fat content assessed by MRI-PDFF (%)

Secondary outcomes

  1. Change from baseline in non-invasive liver fibrosis marker

    Time frame: 48 weeks

    Liver fibrosis assessed by magnetic resonance elastography (kPa)

  2. Change from baseline in markers of liver injury

    Time frame: 48 weeks

    Alanine aminotransferase (ALT) (U/L), aspartate aminotransferase (AST) (U/L), and gamma glutamyl transferase (GGT) (U/L).

  3. Change from baseline in markers of glycemic control

    Time frame: 48 weeks

    Fasting blood glucose (mg/dL)

  4. Change from baseline in Hemoglobin A1C (%)

    Time frame: 48 weeks

    Hemoglobin A1C (%)

  5. Change from baseline in lipoproteins

    Time frame: 48 weeks

    To compare changes in total cholesterol, triglyceride, HDL-cholesterol, and LDL-Total cholesterol (mg/dL), Triglycerides (TG) (mg/dL), high density lipoprotein cholesterol (HDL-C) (mg/dL), Non-HDL-C (mg/dL), and low-density lipoprotein cholesterol (LDL-C) (mg/dL)

  6. Change from baseline in body fat composition assessed by Bioelectrical Impedance Analysis

    Time frame: 48 weeks

    Body fat percentage assessed by Bioelectrical Impedance Analysis

  7. Change from baseline in muscle mass assessed by Bioelectrical Impedance Analysis

    Time frame: 48 weeks

    Muscle mass in kilograms assessed by Bioelectrical Impedance Analysis

  8. Change from baseline in visceral fat assessed by Bioelectrical Impedance Analysis

    Time frame: 48 weeks

    Visceral fat rate assessed by Bioelectrical Impedance Analysis

  9. Change from baseline in wieght in kilograms assessed by Bioelectrical Impedance Analysis

    Time frame: 48 weeks

    Body wieght in kilograms assessed by Bioelectrical Impedance Analysis

Sponsors and collaborators

Lead sponsor

Mahidol University

Other

Registry information

Official study title

Hepatic Elastography-Enhanced Lifestyle Modification in Patients With Metabolic Dysfunction-Associated Steatotic Liver Disease: A Randomized Controlled Trial

Important dates

Study start
2025
Primary completion
2027
Study completion
2027
First posted
Feb 14, 2025
Registry last updated
May 13, 2025

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.

Published trials that share one or more normalized conditions with this study.