Clinical Research Details

A 5-year Longitudinal Observational Study of Patients with Nonalcoholic Fatty Liver (NAFL) or Nonalcoholic Steatohepatitis (NASH)

Study Description

This is an observational research study. Individuals are being asked to be a part of this study because they have non-alcoholic fatty liver disease (NAFLD). There are no required visits or treatments for this study. However, if individual consents to participate, the study sponsor, TARGET PharmaSolutions Inc., (hereafter referred to as “sponsor”), will access the participant's medical record to collect information about the history of the disease and treatment over the last 3 years. In addition, the sponsor will collect medical information from the participant's future medical records for up to 5 years. Participants may also be asked to complete study questionnaires and provide blood samples during the study participation.

Inclusion/Exclusion Criteria

Inclusion Criteria:

  1. 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.
  2. Exclusion Criteria:
  3. Inability to provide informed assent/consent.