Clin2
NCT06160271Worth exploringNot yet recruiting

Using a new scan to measure liver scarring in NASH

Non-alcoholic Steatohepatitis

Part of Digestive system clinical trials.

This study tests if a new imaging agent (68Ga-FAPI-46) can accurately measure liver scarring (fibrosis) in people with NASH, a type of fatty liver disease. It may offer a way to track liver damage without needing repeated biopsies.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 2
Enrollment
72 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You must have had a recent liver biopsy that shows you have or might have NASH (a type of fatty liver disease).
  • You cannot have hepatitis B or C.
  • You cannot have advanced liver cirrhosis with complications like belly fluid or yellowing of the skin.
  • You must not have taken certain medications (like steroids or methotrexate) that can cause fatty liver.
  • You must not have had more than 2 drinks a day (men) or 1 drink a day (women) in the last 5 years.
  • You must be well enough to have a PET scan (a special imaging test).

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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