New french registry tracks rare blood disorders in adults
NCT ID NCT02877706
First seen Jan 11, 2026 · Last updated May 01, 2026 · Updated 17 times
Summary
This study is a national registry in France that collects information from adults newly diagnosed with immune thrombocytopenia (ITP) or autoimmune hemolytic anemia (AIHA). The goal is to better understand these rare blood disorders, track how they progress, and evaluate the real-world safety and effectiveness of treatments. No new treatment is given; researchers simply observe and record data from routine care.
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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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Contacts and locations
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Study contacts
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Contact
Email: •••••@•••••
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Contact
Email: •••••@•••••
Locations
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Service de Médecine Interne
RECRUITINGToulouse, 31000, France
Contact Email: •••••@•••••
Conditions
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