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Imaging the Pancreas With MRI in Type 1 Diabetes

Studies pancreas MRI scans in people with type 1 diabetes and other diabetes types.

Plain-language title generated from the registry record
Registry title: Multicenter Assessment of the Pancreas in Type 1 Diabetes

Key facts

Where
Aurora, Austin, Chicago, and Nashville, United StatesSee the 4 sites

Where in United States

  • University of Colorado, Barbara Davis CenterAurora, United StatesNo longer taking part
  • University of Texas at Austin, Dell Medical SchoolAustin, United StatesNo longer taking part
  • University of Chicago, Kovler Diabetes CenterChicago, United StatesNo longer taking part
  • Vanderbilt University Medical CenterNashville, United StatesNo longer taking part

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Trial details

Who runs it
Vanderbilt University Medical Center
Trial code
NCT03585153
Record updated
23 October 2026
Original description
The overall goal of this research is to develop and validate standard operating procedures (SOP) to assess the human pancreas in individuals with type 1 diabetes (T1D) and other forms of diabetes using advanced, quantitative magnetic resonance imaging (MRI) approaches.Read full original descriptionShow less

Multicenter Assessment of the Pancreas in Type 1 Diabetes

The overall goal of this research is to develop and validate standard operating procedures (SOP) to assess the human pancreas in individuals with type 1 diabetes (T1D) and other forms of diabetes using advanced, quantitative magnetic resonance imaging (MRI) approaches.

Inclusion: Subjects at least 8 years of age; Subjects with T1D must be imaged within 100 days of their date of diagnosis; Subjects must be able to read and provide assent/informed written consent.

Exclusion: Subjects with pancreatitis, cystic fibrosis, pancreatic adenocarcinoma, or neuroendocrine tumors; Subjects who have any type of bioimplant activated by mechanical, electronic, or magnetic means because such devices may be displaced or malfunction; Subjects who have any type of ferromagnetic bioimplant that could potentially be displaced; Subjects who are pregnant or breast-feeding. Urine pregnancy test will be performed on women of child bearing potential who are not practicing appropriate contraception measures or menstruating; Subjects who exhibit significant anxiety and/or claustrophobia; Subjects incapable of giving assent/informed written consent; For controls: subjects who have first degree relatives with T1D.

ClinicalTrials.gov NCT03585153