Large patient registry sheds light on APS and lupus
NCT ID NCT02782039
First seen Nov 01, 2025 · Last updated Apr 29, 2026 · Updated 26 times
Summary
This study created a registry to collect medical information from 868 patients with Anti-Phospholipid Syndrome (APS) and/or Systemic Lupus Erythematosus (SLE). The goal was to better understand these autoimmune diseases by gathering data from affected individuals. No treatments were tested; the focus was on observation and information gathering.
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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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Locations
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Hôpital Claude Huriez
Lille, 59000, France
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Hôpital Cochin
Paris, PARIS, 75014, France
Conditions
Explore the condition pages connected to this study.