New MRI scan could predict liver cancer in NASH patients
NCT ID NCT05165446
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.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 35 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2022
- Expected to finish
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Aug 2026
An estimate. End dates often move.
- Lead sponsor
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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
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18 to 99 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide 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
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Stanford Hospital
Stanford, California, 94305, United States
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Other studies related to the condition(s) this trial covers.
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