Plain-English translation of NCT05824403 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
This is a registry study — a long-term collection of medical information from patients with pancreatic diseases like inflammation or cysts. Researchers are gathering detailed health data to better understand these conditions and improve the tools doctors use to diagnose and monitor them over time.
Some pancreatic conditions carry a risk of becoming cancer, and doctors need better ways to track and diagnose these diseases early. By collecting information from many patients, researchers hope to improve monitoring strategies and help doctors catch problems sooner.
You likely qualify if…
You likely don't qualify if…
As a participant, you would allow researchers to collect and store your medical information related to your pancreatic condition. This typically involves signing consent forms and allowing access to your medical records and test results. There are no experimental medications or procedures — this is purely a data collection study to help improve future care.
AI-generated summary from trial data · Jul 15, 2026 · Not medical advice
France
Enrollment target
~300 participants
Started
November 2023
Primary completion
December 2027
Age range
18 Years and older
Last updated on clinicaltrials.gov in December 2023.
Reach out to the team running this trial. Response times vary — some teams are faster than others.
Central contact
Barbara BOURNET, MD
University Hospital, Toulouse
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.