πŸ›οΈ Verified NIH Record β€’ Updated 2026-08-10

National Liver Cancer Screening Trial (NCT06084234)

🟒 Recruiting Phase4 πŸ“‹ Clinical Research Protocol Sponsor: University of Texas Southwestern Medical Center

🩺 Plain-English Summary (8th-Grade Level)

The National Liver Cancer Screening Trial is an adaptive randomized phase IV Trial comparing ultrasound-based versus biomarker-based screening in 5500 patients with cirrhosis from any etiology or patients with chronic hepatitis B infection. Eligible patients will be randomized in a 1:1 fashion to Arm A using semi-annual ultrasound and AFP-based screening or Arm B using semi-annual screening using GALAD alone. Randomization will be stratified by sex, enrolling site, Child Pugh class (A vs. B), and HCC etiology (viral vs. non-viral). Patients will be recruited from 15 sites (mix of tertiary care and large community health systems) over a 3-year period, and the primary endpoint of the phase IV trial, reduction in late-stage HCC, will be assessed after 5.5 years.

Who can join: Review the eligibility criteria below.

Location: University of Southern California β€” Los Angeles, California

Age range: 18 Years to 85 Years

πŸ§ͺ Interventions in This Study

  • GALAD (DIAGNOSTIC_TEST)
  • Liver Ultrasound with or without AFP (DIAGNOSTIC_TEST)

πŸ“‹ "Do I Qualify?" β€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria β†—

πŸ“ All Participating Trial Locations (19 Sites)

  • University of Southern California β€” Los Angeles, California
  • Stanford University β€” Redwood City, California
  • Kaiser Permanente β€” Roseville, California
  • University of California, San Francisco β€” San Francisco, California
  • Northwestern University β€” Chicago, Illinois
  • Indiana University β€” Indianapolis, Indiana
  • Massachusetts General Hospital β€” Boston, Massachusetts
  • University of Michigan β€” Ann Arbor, Michigan
  • Henry Ford Health System β€” Detroit, Michigan
  • Hennepin Healthcare β€” Minneapolis, Minnesota
  • University of Minnesota β€” Minneapolis, Minnesota
  • The Feinstein Institutes, Northwell Health, Inc. β€” Manhasset, New York
  • University of North Carolina β€” Chapel Hill, North Carolina
  • Case Western Reserve University β€” Cleveland, Ohio
  • The Cleveland Clinic β€” Cleveland, Ohio
  • University of Pennsylvania β€” Philadelphia, Pennsylvania
  • UT Southwestern Medical Center and Parkland Hospital β€” Dallas, Texas
  • Baylor College of Medicine β€” Houston, Texas
  • Virginia Commonwealth University β€” Richmond, Virginia

πŸ“ž Contact the Study Coordinator

Phone: (214) 645-8821

Email: Amit.Singal@UTSouthwestern.edu

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

πŸ’° Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA Β§ 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

πŸ’‘ How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
πŸ›οΈ View Official NIH Record β†—