The Availability of the Enhanced Liver Fibrosis (ELF) Test Affects the Rate of Diagnosis of Nonalcoholic Steatohepatitis (NASH) With Fibrosis in Patients Referred to Hepatology

Last updated: May 6, 2022
Sponsor: University of Kansas Medical Center
Overall Status: Active - Recruiting

Phase

N/A

Condition

Liver Disease

Hepatic Fibrosis

Scar Tissue

Treatment

N/A

Clinical Study ID

NCT05370053
STUDY00145402
  • Ages > 18
  • All Genders

Study Summary

Background: During the hepatology evaluation, vibration-controlled transient elastography (VCTE) is often used as a clinical decision aid to target high-risk patients for liver biopsy. The enhanced liver fibrosis (ELF) test is expected to be approved in the US. We tested the hypothesis that making the ELF results available to the treating hepatologist will result in more appropriate and targeted use of liver biopsy in patients with elevated liver enzymes or fatty liver, and will result in more cases of advanced fibrosis/cirrhosis being diagnosed. Methods: During the hepatology evaluation for elevated liver enzymes or fatty liver at the University of Kansas Medical Center, the hepatologists (8 total) make a clinical decision on whether patients shall receive VCTE. At the end of the clinic visit, patients were enrolled and randomized to receiving an ELF test. Patients with liver biopsy within the last five years or decompensated cirrhosis were excluded. The primary outcome is the rate of a diagnosis of F3-4 fibrosis based on liver biopsy or clinical diagnosis of cirrhosis with the initiation of hepatocellular carcinoma surveillance. Four hundred fifty patients are to be enrolled over two years.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Patients from hepatology clinic undergoing new evaluation for NAFLD.

Exclusion

Exclusion Criteria:

  • Patients with liver biopsy within the last five years or decompensated cirrhosis wereexcluded. Patients known to have other liver diseases were also excluded. Patientsconsuming > 14 drinks in the past 6 months were excluded. Patients may be subsequentlyfound to have positive viral or autoimmune serologies after enrollment because theserology result is typically not available at the time of enrollment. These patientswill be excluded from the analysis.

Study Design

Total Participants: 450
Study Start date:
September 01, 2020
Estimated Completion Date:
December 01, 2022

Connect with a study center

  • University of Kansas Medical Center

    Kansas City, Kansas 66160
    United States

    Active - Recruiting

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