French doctors track rare genetic pancreatitis to unlock cancer clues
NCT ID NCT07413029
Summary
This study aims to better understand hereditary pancreatitis, a rare genetic condition caused by mutations in the PRSS1 gene. Researchers will follow 800 patients in France over time to learn about the disease's natural course, track the risk of developing pancreatic cancer, and see how it affects patients' quality of life. The goal is to gather knowledge to improve future care for people with this condition.
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Contacts and locations
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Study contacts
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Contact
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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REBOURS
RECRUITINGClichy-sous-Bois, France
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
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