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NCT03585153Enrolling by invitation

Multicenter Assessment of the Pancreas in Type 1 Diabetes

Source: ClinicalTrials.gov · Last updated 23 Oct 2026

Brief summary (registry, in English)

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.

Status (registry)
Enrolling by invitation
Study type
Observational
Enrollment
250 (estimated)
First submitted
18 Jun 2018
Start date
19 Feb 2014
Primary completion date
Dec 2028
Lead sponsor
Vanderbilt University Medical Center
NCT number
NCT03585153

What you commit to

  • Study type: Observational
  • Planned participants: 250
  • From 19 Feb 2014 to the primary completion date, Dec 2028
  • 5 sites in 2 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • 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

Who the study is looking for

  • 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

Age in the registry: 8 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (5)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
St. Vincent's Institute of Medical Research
Coordinator of this site? Confirm its status
MelbourneAustraliaUnknown status
University of Colorado, Barbara Davis Center
Coordinator of this site? Confirm its status
AuroraUnited StatesUnknown status
University of Texas at Austin, Dell Medical School
Coordinator of this site? Confirm its status
AustinUnited StatesUnknown status
University of Chicago, Kovler Diabetes Center
Coordinator of this site? Confirm its status
ChicagoUnited StatesUnknown status
Vanderbilt University Medical Center
Coordinator of this site? Confirm its status
NashvilleUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.