Plain-English translation of NCT05714111 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
Read our Pancreatic Cancer research guide →This is a registry study — a database where doctors collect medical imaging scans and health information from patients with pancreatic cancer or pancreatic disease. Researchers will use this information to learn how imaging scans help doctors make treatment decisions and predict how well patients do over time.
Pancreatic cancer is a serious disease, and doctors need better ways to use imaging (like CT scans) to understand which patients will respond to treatment and how to monitor them. By collecting real-world data from many patients, doctors can improve how they use these imaging tools to help future patients.
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You would allow researchers to access your imaging scans (like CT or MRI images) and medical records that you've already had done as part of your regular pancreatic cancer care. This is a passive study — you won't need to come in for extra visits or take new medications. Doctors will simply review your scans and follow how you respond to your regular treatment over time.
AI-generated summary from trial data · Aug 11, 2026 · Not medical advice
Italy
Sponsor
IRCCS San Raffaele
Enrollment target
~1,300 participants
Started
March 2022
Primary completion
March 2027
Age range
18 Years and older
Last updated on clinicaltrials.gov in September 2026.
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.