New french registry tracks rare blood disorders to improve care
NCT ID NCT02877706
First seen Jan 11, 2026 · Last updated Jun 13, 2026 · Updated 24 times
Summary
This study is a national registry in France that collects information on adults newly diagnosed with immune thrombocytopenia (ITP) or autoimmune hemolytic anemia (AIHA). It aims to describe how these diseases progress and how well treatments work in real life. No new treatment is given; researchers simply observe and record data from 1,500 participants over time.
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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
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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