120 Participants Needed

Ultrasound for Fatty Liver Disease in Children

AA
GT
Overseen ByGage Tanzman
Age: < 65
Sex: Any
Trial Phase: Academic
Sponsor: University of California, San Diego
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial explores new ultrasound techniques to evaluate liver disease in children without invasive methods. Researchers aim to compare these advanced techniques with traditional methods like MRI scans and adapt them for portable ultrasound devices. Children aged 9 to 18 with risk factors for MASLD (a type of liver disease related to fat buildup) may qualify for this study. Participants must complete all study procedures and have no other liver conditions. As an unphased study, this trial offers participants the chance to contribute to innovative research that could lead to less invasive diagnostic options for liver disease in children.

Why are researchers excited about this trial?

Researchers are excited about using quantitative ultrasound to assess steatotic liver disease in children because it offers a non-invasive and radiation-free method to evaluate liver fat. Unlike traditional methods like liver biopsies, which are invasive and can be painful, this ultrasound technique is safe and comfortable for young patients. Additionally, it provides real-time results, making it easier for doctors to monitor liver health and potentially catch problems earlier. This approach could revolutionize how pediatric liver disease is diagnosed and managed, making it less stressful for both kids and their families.

Who Is on the Research Team?

JB

Jeffrey B Schwimmer, MD

Principal Investigator

University of California, San Diego

CB

Claude B Sirlin, MD

Principal Investigator

University of California, San Diego

Are You a Good Fit for This Trial?

Inclusion Criteria

I have risk factors for metabolic-associated fatty liver disease.
I can and will sign a consent form.
I am willing to sign a consent form.
See 1 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Ultrasound Evaluation

Participants undergo ultrasound exams using full-size or POCUS devices to develop and test QUS models

5 years

Follow-up

Participants are monitored for safety and effectiveness after ultrasound evaluation

4 weeks

What Are the Treatments Tested in This Trial?

How Is the Trial Designed?

1

Treatment groups

Experimental Treatment

Group I: CohortExperimental Treatment5 Interventions

Find a Clinic Near You

Who Is Running the Clinical Trial?

University of California, San Diego

Lead Sponsor

Trials
1,215
Recruited
1,593,000+

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Collaborator

Trials
2,513
Recruited
4,366,000+

GE Healthcare

Industry Sponsor

Trials
307
Recruited
634,000+
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Fotis Vlachos

GE Healthcare

Chief Marketing Officer since 2024

PhD in Molecular Biology and Biochemistry from the University of Massachusetts, MBA from the Wharton School of the University of Pennsylvania

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Peter J. Arduini

GE Healthcare

Chief Executive Officer since 2022

MBA from Northwestern University, BSc in Marketing from Susquehanna University

Virginia Polytechnic Institute and State University

Collaborator

Trials
162
Recruited
26,900+