The T1D Exchange Clinic Registry is coordinated by the Jaeb Center for Health Research and funded by the Leona M. and Harry B. Helmsley Charitable Trust through the Helmsley Type 1 Diabetes Program. Currently, 66 clinics are participating in the T1D Exchange Clinic Registry. The milestone of reaching our goal of enrolling 25,000 participants with type 1 diabetes was achieved in June 2012.

The overall objective of the T1D Exchange Clinic Registry is to improve the care of persons with type 1 diabetes (T1D) through sharing of best practices by collecting data in a common data repository. The registry aims to collect core clinical and laboratory data on persons with T1D in order to:

  1. Address pertinent clinical issues
  2. Conduct exploratory/hypothesis-generating analyses
  3. Categorize participants for future clinical studies

To request more information, data, or submit study ideas contact us.


For more information about the registry and other T1D Exchange initiatives, view our flyer.