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The Registry is designed to be patient-centered in its approach as part of its mission to be a truly inclusive, representative, and transparent research effort that has the potential to advance care for people with type 1 diabetes.
Researchers examined the cardiovascular risk factors of those enrolled in the T1D Exchange Clinic Registry and the German/Austrian DPV registry. The findings were unveiled at the American Diabetes Association 79th Annual Scientific Sessions in San Francisco.
A survey of T1D Exchange Clinic Registry participants found that some teens may be materially less likely than their younger peers to handle blood sugar emergencies. The findings were presented at the ADA 79th Scientific Sessions in San Francisco.
This pioneering effort provides a mobile-friendly platform for people throughout the U.S. to participate online and share information about their type 1 diabetes in order to help researchers develop more targeted and effective approaches to treating and living with the disease.