Plain-English translation of NCT06782230 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
Researchers are building a coordinated system across Italy to collect and store biological samples (like blood) from people with rare diseases. The goal is to create a shared network of sample banks so that future researchers have access to high-quality materials for studying rare cardiovascular and neurological conditions. This makes it easier for scientists to conduct collaborative studies without requiring patients to travel long distances.
Rare diseases affect small numbers of people, which makes it very difficult for researchers to gather enough biological samples for meaningful studies. By creating a connected network of collection centers, this project overcomes the scarcity of samples and enables scientists across Italy and internationally to work together on finding better treatments.
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You would visit one of the participating collection centers in your region and provide a biological sample (typically blood). The center will collect this sample using standard procedures, store it safely, and link it with basic health information. Your sample becomes part of a national database that researchers can access to study rare diseases—but your identity is protected.
AI-generated summary from trial data · Jun 5, 2026 · Not medical advice
Italy
Enrollment target
~800 participants
Started
August 2024
Primary completion
August 2026
Last updated on clinicaltrials.gov in January 2025.
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Central contact
Rosanna Cardani, PhD
IRCCS Policlinico S. Donato
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