Tracking the journey of infants with devastating genetic epilepsy
NCT ID NCT04802135
Summary
This study is creating a registry to track 200 infants with a rare, severe genetic epilepsy called KCNQ2-related epileptic encephalopathy. Researchers will follow these children long-term to better understand how their seizures, brain activity, and development progress over time. The goal is to gather detailed information that could help guide future treatments for this condition.
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Contacts and locations
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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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APHP Pitié Salpêtrière
RECRUITINGParis, France
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APHP Robert Debré
NOT_YET_RECRUITINGParis, France
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CHRU Lille
NOT_YET_RECRUITINGLille, France
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CHRU Strasbourg
NOT_YET_RECRUITINGStrasbourg, France
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CHU Angers
NOT_YET_RECRUITINGAngers, France
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CHU Bordeaux
NOT_YET_RECRUITINGBordeaux, France
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CHU Brest
NOT_YET_RECRUITINGBrest, France
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CHU Limoges
NOT_YET_RECRUITINGLimoges, France
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CHU Montpellier
NOT_YET_RECRUITINGMontpellier, France
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CHU Rennes
NOT_YET_RECRUITINGRennes, France
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CHU Toulouse
NOT_YET_RECRUITINGToulouse, France
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CHU Tours
NOT_YET_RECRUITINGTours, France
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Hospices Civils Lyon
NOT_YET_RECRUITINGLyon, France
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Contact
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Hôpital La Timone
RECRUITINGMarseille, 13005, France
Contact Phone: •••-•••-•••• Email: •••••@•••••
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Hôpital Necker
NOT_YET_RECRUITINGParis, France
Contact Email: •••••@•••••
Conditions
Explore the condition pages connected to this study.