Italy launches massive registry to track rare hereditary polyposis
NCT ID NCT07461246
First seen Mar 11, 2026 · Last updated May 27, 2026 · Updated 10 times
Summary
This study is creating a national Italian registry of 1500 people with familial adenomatous polyposis (FAP) and related conditions. Researchers will collect medical history, genetic data, and treatment outcomes to better understand how the disease progresses and how care can be improved. The goal is to standardize management and support future research, but no new treatment is being tested.
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Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Locations
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Fondazione IRCCS Istituto Nazionale dei Tumori
Milan, 20133, Italy
Conditions
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