NCT06826807

Brief Summary

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.

Trial Health

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
92

participants targeted

Target at P50-P75 for not_applicable

Timeline
13mo left

Started May 2025

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
enrolling by invitation

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress48%
May 2025Jun 2027

First Submitted

Initial submission to the registry

January 28, 2025

Completed
17 days until next milestone

First Posted

Study publicly available on registry

February 14, 2025

Completed
3 months until next milestone

Study Start

First participant enrolled

May 12, 2025

Completed
1.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2027

Expected
5 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2027

Last Updated

May 13, 2025

Status Verified

May 1, 2025

Enrollment Period

1.6 years

First QC Date

January 28, 2025

Last Update Submit

May 12, 2025

Conditions

Keywords

Lifestyle modificationMASLDtransient elastography

Outcome Measures

Primary Outcomes (1)

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

    Hepatic fat content assessed by MRI-PDFF (%)

    48 weeks

Secondary Outcomes (9)

  • Change from baseline in non-invasive liver fibrosis marker

    48 weeks

  • Change from baseline in markers of liver injury

    48 weeks

  • Change from baseline in markers of glycemic control

    48 weeks

  • Change from baseline in Hemoglobin A1C (%)

    48 weeks

  • Change from baseline in lipoproteins

    48 weeks

  • +4 more secondary outcomes

Study Arms (2)

Experimental: Active Comparator: Regular hepatic elastography monitoring to encourage dietary modifi

EXPERIMENTAL

• MASLD patient will undergo regular hepatic elastography monitoring to assess liver fat composition and receive feedback to encourage dietary modifications and increased physical activity.

Other: Regular monitoring with transient elastography

No Intervention: Placebo comparator: standard care (counselling for dietary modifications and increa

NO INTERVENTION

The control group will receive standard care (counselling for dietary modifications and increased physical activity) without elastography monitoring.

Interventions

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

Experimental: Active Comparator: Regular hepatic elastography monitoring to encourage dietary modifi

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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.

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Faculty of Medicine Siriraj Hospital, Mahidol University

Bangkoknoi, Bangkok, 10700, Thailand

Location

Related Publications (39)

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MeSH Terms

Conditions

Metabolic SyndromeNon-alcoholic Fatty Liver DiseaseInsulin ResistanceCardiovascular Diseases

Condition Hierarchy (Ancestors)

HyperinsulinismGlucose Metabolism DisordersMetabolic DiseasesNutritional and Metabolic DiseasesFatty LiverLiver DiseasesDigestive System Diseases

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: The intervention group will undergo regular hepatic elastography monitoring to assess liver fat composition and receive feedback to encourage dietary modifications and increased physical activity. The control group will receive standard care without elastography monitoring.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

January 28, 2025

First Posted

February 14, 2025

Study Start

May 12, 2025

Primary Completion (Estimated)

January 1, 2027

Study Completion (Estimated)

June 1, 2027

Last Updated

May 13, 2025

Record last verified: 2025-05

Data Sharing

IPD Sharing
Will not share

Locations