New model aims to speed up rare disease diagnoses
NCT ID NCT07558213
First seen May 05, 2026 · Last updated May 16, 2026 · Updated 1 time
Summary
This study is testing a new way to care for people with rare diseases. It brings together specialists, new technologies like genetic testing, and better coordination between hospitals and local services. The goal is to help 136 patients get a faster diagnosis and reduce unnecessary hospital visits.
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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 Policlinico Universitario A. Gemelli Irccs
Roma, 00168, Italy
Conditions
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