Groundbreaking study seeks genetic clues to infant seizures
NCT ID NCT06701084
First seen Apr 29, 2026 · Last updated May 21, 2026 · Updated 5 times
Summary
This study aims to find new genetic causes of epilepsy in babies and understand how a genetic diagnosis helps families. Researchers will enroll 600 infants who had their first seizure before 12 months old. They will use genetic testing and track development, seizure control, and family experiences to see the benefits of early diagnosis.
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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: •••••@•••••
Locations
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Boston Children's Hospital
RECRUITINGBoston, Massachusetts, 02115, United States
Contact
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
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