Massive french sarcoma database aims to unlock secrets of rare cancers
NCT ID NCT03978039
First seen Nov 01, 2025 · Last updated Jun 10, 2026 · Updated 34 times
Summary
This study is creating a large national database in France to collect medical and biological information from people diagnosed with sarcoma, a rare type of cancer. By gathering data from up to 150,000 participants, researchers hope to better understand how sarcomas are treated and what factors affect patient outcomes. The database will help doctors improve care for future patients.
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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
Phone: •••-•••-•••• Email: •••••@•••••
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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Centre Léon Bérard
RECRUITINGLyon, France
Contact
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Institut Bergonié, Comprehensive Cancer Center
RECRUITINGBordeaux, France
Contact
Contact
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Institut Gustave Roussy, Comprehensive Cancer Center
RECRUITINGVillejuif, France
Contact
Conditions
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