Clinical trial Recruiting at 1 site Observational

New MRI methods to measure metabolism and predict outcomes in metabolic-associated fatty liver disease

Official title: To Explore the Value of New MR Technology in Non-invasive Quantitative Assessment of Systemic Metabolism, Disease Status and Prognosis in Patients With Metabolic-Associated Fatty Liver Disease

Run by Tongji Hospital · NCT07149571 · Data updated 2026-11-12

This project tests whether new MRI techniques can measure body metabolism and help predict disease status and prognosis for people with metabolic-associated fatty liver disease.

More Nonalcoholic Fatty Liver Disease trials

Quick facts

Study typeObservational
SexAll
Enrollment500 (estimated)
SponsorTongji Hospital
Academic / other
Locations1 site (Wuhan, Hubei)
StatusRecruiting
StartedApril 1, 2025
Main results expectedDecember 1, 2032
Study endsDecember 31, 2032
Registry record updatedSeptember 2, 2025
Trial IDNCT07149571 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

People of any age or gender who are clinically suspected or diagnosed with metabolism-related (metabolic-associated) fatty liver disease and who can undergo MR imaging and give informed consent are eligible.

Probably not a fit

Patients who cannot have MRI (for example due to incompatible implants, severe claustrophobia, or other contraindications) or who are seeking direct experimental treatment rather than imaging biomarker data are unlikely to receive direct benefit from participation.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is an observational study that collects clinical, imaging, laboratory, and pathological data from people with metabolism-related fatty liver disease. Participants undergo MR imaging and the resulting scans are processed with advanced image-analysis software to extract quantitative imaging parameters and body-composition metrics. Investigators will look for links between those imaging measures, metabolic disorders, and disease severity to support non-invasive diagnosis, treatment monitoring, and prognosis prediction. The goal is to generate imaging biomarkers that can help guide clinical care and improve patient outcomes.

Why it matters

Potential benefit: If successful, the approach could provide non-invasive MRI-based markers to help diagnose, track treatment response, and predict outcomes for patients with MAFLD.

How similar studies have gone: Previous work using MRI biomarkers such as proton density fat fraction and MR elastography has shown promise for diagnosing and staging fatty liver, but applying newer MR techniques specifically to quantify systemic metabolism and predict long-term prognosis is a newer and still-developing area.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Patients with MR examination are clinically suspected or diagnosed with metabolism-related fatty liver disease;
2. Age/gender: unlimited;
3. Patients who voluntarily participate in clinical trials and sign written subject informed consent

Exclusion Criteria:

1. Clinical suspicion or diagnosis of metabolism-related fatty liver disease and having been prescribed an MR examination;
2. Voluntarily participation in the study and provision of written informed consent.

Where it's running

  • Tongji hospital
    Wuhan, Hubei, China
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.