Groundwork laid for future treatments of rare brain disorders
NCT ID NCT06555965
Summary
This study aims to learn more about two rare genetic brain disorders, STXBP1 and SYNGAP1, which cause severe developmental delays and epilepsy. Researchers will follow 600 participants for up to five years, tracking their symptoms and quality of life through regular check-ups and assessments. The information collected will help design future clinical trials for potential treatments.
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
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Locations
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Children's Hospital Colorado
RECRUITINGAurora, Colorado, 80011, United States
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Stanford Medicine Children's Health
RECRUITINGPalo Alto, California, 94304, United States
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Texas Children's Hospital
RECRUITINGHouston, Texas, 77030, United States
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The Children's Hospital of Philadelphia
RECRUITINGPhiladelphia, Pennsylvania, 19403, United States
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Weill Cornell Medicine
RECRUITINGNew York, New York, 10065, United States
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Conditions
Explore the condition pages connected to this study.