Pancreatic cancer risk registry for high-risk families
Part of Cancer, Digestive system, Genetic & congenital, Hormones & metabolism, Skin clinical trials.
This study builds a registry of people with a higher-than-average risk of pancreatic cancer, based on family history or inherited gene conditions. If you join the extra imaging follow-up, it helps your care team monitor risk earlier.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You have a family history with at least two relatives who had pancreatic cancer, including a close relative (first-degree) and up to a third-degree relative
- OR you have a known inherited gene change such as BRCA1, BRCA2, p16, or PALB2, plus at least one affected first- or second-degree relative
- OR you have certain inherited syndromes (FAMMM or Peutz-Jeghers)
- OR you have specific inherited types of pancreatitis (PRSS-1, CFTR, or SPINK-1 related)
- OR you have Lynch syndrome and at least one first- or second-degree relative with pancreatic cancer
- You must not be pregnant
Quick eligibility check
Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.
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