Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06184152

CEUS vs. AMRI for HCC Detection in Patients With Indeterminate Liver Nodules

Led by University of Texas Southwestern Medical Center · Updated on 2025-08-05

600

Participants Needed

2

Research Sites

261 weeks

Total Duration

On this page

Sponsors

U

University of Texas Southwestern Medical Center

Lead Sponsor

U

University of Michigan

Collaborating Sponsor

AI-Summary

What this Trial Is About

The study will be conducted at the following locations: 1. UT Southwestern Medical Center 2. Parkland Health and Hospital System 3. University of Michigan Investigators will prospectively compare the performance of dynamic contrast enhanced abbreviated MRI (AMRI) and contrast-enhanced ultrasound for early-stage HCC detection in patients with indeterminate liver nodules.

CONDITIONS

Official Title

CEUS vs. AMRI for HCC Detection in Patients With Indeterminate Liver Nodules

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults 18 years old and above
  • Child A or B cirrhosis from any cause with at least one indeterminate liver nodule on 4-phase CT, contrast-enhanced MRI, or contrast-enhanced ultrasound but no HCC at baseline
Not Eligible

You will not qualify if you...

  • History of liver transplantation
  • Current or prior hepatocellular carcinoma (LR-5 or biopsy proven)
  • Other liver cancers including cholangiocarcinoma
  • Any active cancer outside the liver
  • Significant other serious health conditions with limited life expectancy, such as stage D congestive heart failure
  • Contraindications to contrast-enhanced MRI or ultrasound, including MR-unsafe implanted devices or severe claustrophobia

AI-Screening

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Trial Site Locations

Total: 2 locations

1

University of Michigan

Ann Arbor, Michigan, United States, 48109

Actively Recruiting

2

University of Texas Southwestern Medical Center

Dallas, Texas, United States, 75390

Actively Recruiting

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Research Team

L

Lisa Quirk, MS/MPH

CONTACT

S

Sneha Deodhar, MS

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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