New study paves way for future treatments in rare brain disorder
NCT ID NCT06018519
First seen Jan 04, 2026 · Last updated May 14, 2026 · Updated 20 times
Summary
This study looks at people with creatine transporter deficiency, a rare genetic condition that causes intellectual disability, seizures, and movement problems. Researchers want to find the best tests and tools to measure changes in patients' abilities, since many standard tests don't work well for them. The goal is to prepare for future clinical trials of new treatments by identifying reliable outcome measures.
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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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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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Woman, mother and child hospital, Hospices Civils de Lyon
RECRUITINGBron, 69500, France
Contact Phone: •••-•••-•••• Email: •••••@•••••
Contact
Conditions
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