Plain-English translation of NCT04427189 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
Read our Type 1 Diabetes research guide →The SWEET-Registry is a worldwide study that gathers real medical information from children and teens with type 1 diabetes. By collecting data from many diabetes centers across different countries, researchers hope to understand which treatment approaches help children do best and reduce long-term complications of diabetes.
Children with diabetes deserve the same chances to grow, learn, and thrive as other kids. This study exists to figure out the best ways to treat diabetes in young people so they can live fuller lives and avoid serious health problems later on.
You likely qualify if…
You likely don't qualify if…
You don't need to do anything special—this is a 'real-world' study, meaning your doctor will treat your diabetes as usual. Your local diabetes clinic will share your medical records (including blood sugar readings, medications, and visit notes) with the research team twice a year. The information is kept anonymous and combined with data from thousands of other young people with diabetes to help researchers find the best care approaches.
AI-generated summary from trial data · Jun 19, 2026 · Not medical advice
Germany
Collaborators
SWEET e.V
Enrollment target
~100,000 participants
Started
April 2008
Primary completion
April 2028
Last updated on clinicaltrials.gov in October 2024.
Reach out to the team running this trial. Response times vary — some teams are faster than others.
Central contact
Olga Prof. Kordonouri, MD
Kinderkrankenhaus auf der Bult
Tell us you're interested and we'll help connect you with the research team. We'll walk you through what to expect first — no email needed to get started.