Family study aims to unlock secrets of rare autoimmune disease
NCT ID NCT07343115
First seen Jan 16, 2026 · Last updated Apr 30, 2026 · Updated 13 times
Summary
This study looks at families where more than one person has systemic scleroderma, a rare autoimmune disease. By studying these families, researchers hope to find clues about how the disease develops and progresses. The study involves 20 adults with the condition and their first-degree relatives. No new treatments are being tested; instead, the goal is to gather information that could lead to better therapies in the future.
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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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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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Service de Médecine interne et Immunologie clinique - CHU de Strasbourg - France
RECRUITINGStrasbourg, 67091, France
Contact Phone: •••-•••-•••• Email: •••••@•••••
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