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6 years or older
TARGET-NASH is a longitudinal observational cohort study of patients being managed for NAFL or NASH in usual clinical practice. TARGET-NASH will create a research registry of patients with NAFL or NASH within academic and community real-world practices in order to assess the safety and effectiveness of current and future therapies.
Who can participate
Adults and children (age 2 or older) being managed or treated for nonalcoholic fatty
liver disease. Diagnosis is based on the clinical judgement of the care provider.
Inability to provide written informed assent/consent
Simultaneous enrollment in another registry, study, or clinical trial where NASH
treatment outcomes are reported, except where approved or conducted as an adjunct
project of TARGET-NASH. If a participant elects to enroll in an interventional
clinical trial during their enrollment in TARGET-NASH, records submissions for the
participant will be put 'on hold' for the trial duration. When participation in the
trial is complete, records submissions for TARGET-NASH will resume.