Plain-English translation of NCT05845801 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
This is a research registry—a database—that collects medical and genetic information from people diagnosed with pancreatic cancer at age 55 or younger. Researchers will use this information to better understand the disease in younger patients and to design and test new treatments in the future.
Pancreatic cancer in younger adults may behave differently than in older patients, and doctors need more information to develop better treatments tailored to this group. This registry brings together data from many young patients in one place so researchers can spot patterns and test new ideas.
You likely qualify if…
You likely don't qualify if…
You will be asked to share your medical records, pathology reports, and genetic test results with the registry. Researchers may also track your health outcomes and survival over time. There is no experimental treatment involved—you are simply contributing your information to help build a database that will guide future pancreatic cancer research.
AI-generated summary from trial data · Aug 11, 2026 · Not medical advice
Italy
Enrollment target
~3,000 participants
Started
December 2022
Primary completion
September 2052
Age range
18 Years – 55 Years
Last updated on clinicaltrials.gov in May 2023.
Reach out to the team running this trial. Response times vary — some teams are faster than others.
Central contact
Fabio Casciani
Azienda Ospedaliera Universitaria Integrata Verona
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.