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Completed

NCT Number: NCT03674528

Technical Validation of MR Biomarkers of Obesity-Associated NAFLD

The overall goal of this collaborative research program is to develop, validate and translate advanced quantitative magnetic resonance (MR) biomarkers of obesity-associated non-alcoholic fatty liver disease (NAFLD). This protocol represents the research plan for two distinct phases. The first phase is an optimization phase. The second phase is designed to complete a rigorous test of conventional and advanced MRE techniques. Complementary anthropometric, laboratory, and MR measures will also be collected to characterize the cohort and identify factors that affect MRE performance

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

University of California, San Diego, La Jolla, California, United States

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About this study

The long-term objective of this research is to improve the health of the millions of Americans with or at risk for NAFLD, the most common chronic liver disease and most rapidly growing indication for liver transplantation in the United States. To achieve this objective, an advanced MR-based imaging method will be used to measure liver "stiffness" which is an early sign of disease. This technique has been previously developed and validated and ready to be used for further research. This current protocol will extend previous work by optimizing and validating advanced 2 dimensional and 3 dimensional-magnetic resonance elastography (MRE) methods as non-invasive biomarkers of hepatic inflammation and fibrosis in obese patients at risk for non-alcoholic steatohepatitis (NASH), the histologically more aggressive subset of NAFLD.

Per Amendment approved 4/8/22: MRE exams will be conducted using a PDFF Pocket Phantom purchased by the UCSD from Calimetrix. This phantom consists of vials with known fat fraction which are captured when taking images of the liver. The known fat fractions provide an independent reference and are used for quality assurance purposes.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

(Phase 1 and 2 participants)

  • Age of at least 18 years
  • Severely obese (BMI ≥ 35 kg/m2) patient

Inclusion criteria

(Phase 2 participants only)

  • Cleared for weight-loss surgery
  • Willing and able to complete all safety and follow-up procedures
  • Willing to allow for the banking of biological samples

Exclusion criteria

(Phase 1 and 2 participants)

  • Contraindications to MRI
  • Girth or weight that exceeds scanner capacity
  • Women of childbearing potential that are pregnant or will be attempting to become pregnant during the study duration.

Exclusion criteria

(Phase 2 participants only)

  • Known liver malignancies
  • Regular & excessive alcohol consumption within 2 years prior to recruitment
  • Use of steatogenic or hepatotoxic drugs
  • Clinical or laboratory evidence of liver disease other than Nonalcoholic fatty liver disease (NAFLD)/ Nonalcoholic steatohepatitis (NASH) (e.g. HCV Ab, HBV Ab, ceruloplasmin)
  • The subject has increased bleeding risk (i.e., decreased platelets, von Willebrand disease)

Treatment and study plan

Magnetic Resonance Elastography (MRE)

Other

The MRE scan will several breath holds and will take approximately 30 minutes to complete.

Other names: MRI

Liver biopsy

Diagnostic Test

Subjects undergoing WLS will be asked to allow for liver biopsy samples to be collected during their surgical procedure. The collection of these samples will take approximately 5 minutes to complete.

Other names: Intraoperative Biopsy

Primary outcomes

  1. Optimization of MRE for 2 dimensional and 3 dimensional methods

    Time frame: Up to 24 months

    Optimize MRE wave-field generation in this subject population to maximize the area of invertible shear waves in the liver into interpretable shear stiffness maps.

Sponsors and collaborators

Lead sponsor

University of Wisconsin, Madison

Other

Collaborators

  • GE Healthcare
  • National Center for Advancing Translational Sciences (NCATS)
  • National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
  • Pfizer
  • Siemens Medical Solutions

Registry information

Official study title

Technical Validation of Magnetic Resonance Biomarkers of Obesity-Associated Non-Alcoholic Fatty Liver Disease

Acronym: NAFLD

Important dates

Study start
2018
Primary completion
2024
Study completion
2024
First posted
Sep 17, 2018
Registry last updated
Sep 19, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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