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New MRI scan could predict liver cancer in NASH patients

NCT ID NCT05165446

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing This study
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests a new, longer MRI scan that measures liver stiffness and viscosity to see if it can identify NASH patients at higher risk for liver cancer. About 35 adults with NASH and early-stage liver scarring will participate. The goal is to improve early detection, not to treat the disease.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

About 35 people

The number the study aims to enrol. It can still change while the study runs.

Started

Jan 2022

Expected to finish

Aug 2026

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

The study will include one group of healthy subjects and two groups with 15 patients each which will enroll in parallel, one group with type 2 diabetes mellitus (T2DM), and one group without DM.

Ages

18 to 99 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: 1. Male or non-pregnant/non-lactating women ≥ 18 years of age 2. Diagnosis of NASH 3. Diagnosis of pre-cirrhotic fibrosis (F1-F3), diagnosed as per standard of care (history, exam, laboratory tests, Fibroscan, within 6 months of enrollment) 4. Na-MELD \< 9: The Na-MELD (sodium-Model for End Stage Liver Disease) score is routinely used to assess liver synthetic function and life expectancy. Patients with Na-MELD\<9 have less than 1.9% 3 months liver-related mortality risk, and their liver synthetic function is normal. 5. Groups both with and without T2DM will be enrolled. 6. Women of childbearing potential must agree to at least two methods of contraception. 7. Will not participate in any other clinical trial for the duration of the study 8. Will not consume alcohol for the duration of the study 9. If on vitamin E, pioglitazone or any anti diabetic treatment prior to the study, will have been on stable therapies for 6 months prior to enrolment. 10. Able to undergo 3 Tesla MRI and complete MRI screening form 11. Ability to understand and the willingness to sign a written informed consent document. 12. ECOG or Karnofsky Performance Status will be not be employed Exclusion Criteria: 1. Presence of any other form of liver disease, including viral hepatitis, autoimmune hepatitis, alcoholic liver disease, genetic causes of chronic liver disease, cardiogenic liver disease, and HIV positivity (can cause liver fibrosis). 2. ALT\>300 U/l 3. Total serum bilirubin ≥ to 1.3 mg/dL (Gilbert's Syndrome patients are excepted) 4. International Normalized Ratio (INR) ≥ 1.3 5. MELD\>9 6. Serum creatinine \>2.0mg/dl 7. Known alcohol abuse or alcohol use disorder (AUDIT profile and/or pos. urine ethylglucuronide): * \>20 g/day for women * \>30 g/day for men 8. Active substance abuse 9. Platelet count ≤100//mm3 10. Hemoglobin \<11 g/dl in females or \<12 g/dl in males 11. Presence/history of HCC, or other primary or metastatic cancer to the liver. 12. History of liver transplantation 13. History of bariatric surgery 14. History of inflammatory bowel disease 15. History of advanced pulmonary disease 16. Any concerns regarding compliance by enrolling physician 17. Pregnant or lactating women. 18. Presence of cardiac implantable electronic device (CIED) 19. History of CIED with retained leads 20. Presence of any metallic foreign body that is unsafe for the MRI environment 21. Inability to undergo MRI based on responses to the MRI screening form 22. History of claustrophobia or the need for sedation to undergo MRI

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Stanford Hospital

    Stanford, California, 94305, United States

More trials for these conditions

Other studies related to the condition(s) this trial covers.