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Search / Trial NCT02025543

Confounder-Corrected Quantitative MRI Biomarker of Hepatic Iron Content

Launched by UNIVERSITY OF WISCONSIN, MADISON · Dec 27, 2013

Trial Information

Current as of June 26, 2025

Enrolling by invitation

Keywords

Mri Iron Overload

ClinConnect Summary

This multi-center, multi-vendor study will validate a rapid magnetic resonance-based confounder-corrected R2\* mapping method as a quantitative imaging biomarker of liver iron concentration (LIC). Excessive accumulation of iron in various organs, including the liver, which affects both adult and pediatric populations, is toxic and requires treatment aimed at reducing body iron stores. Measurement of LIC is critical for detection and staging of iron overload, and for monitoring iron-reducing chelator therapies that are expensive and have side effects. Magnetic Resonance Imaging (MRI) is a wi...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • know or suspected iron overload
  • minimum age: Stanford- 8years , University of Wisconsin - 10 years, John Hopkins follow- 10 years, University of Texas-Southwestern - 18 years
  • Exclusion Criteria:
  • contraindication to magnetic resonance imaging

About University Of Wisconsin, Madison

The University of Wisconsin-Madison is a leading research institution renowned for its commitment to advancing healthcare through innovative clinical trials. With a strong emphasis on interdisciplinary collaboration, the university leverages its extensive resources, including cutting-edge facilities and a diverse pool of expert researchers, to conduct rigorous studies that address critical health challenges. The institution's focus on translating research findings into practical applications fosters the development of new treatments and interventions, ultimately contributing to improved patient outcomes and public health initiatives. As a sponsor of clinical trials, the University of Wisconsin-Madison is dedicated to upholding the highest ethical standards and ensuring participant safety throughout the research process.

Locations

Palo Alto, California, United States

Baltimore, Maryland, United States

Dallas, Texas, United States

Madison, Wisconsin, United States

Patients applied

0 patients applied

Trial Officials

Scott Reeder

Principal Investigator

University of Wisconsin, Madison

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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