New study tracks how dravet syndrome changes over time

NCT ID NCT07251673

First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study follows 50 children and young adults with Dravet syndrome caused by SCN1A gene mutations over four years. Researchers will use standard tests to measure changes in thinking, movement, and daily skills. They will also look for chemical markers in the blood that might relate to how the disease progresses. The goal is to better understand the natural course of the condition, which could help improve future treatments and clinical trial design.

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

What this could lead to

If successful, this study could provide a clearer picture of how Dravet syndrome develops over time, helping design better future treatments and clinical trials.

What could go wrong

This is an observational study, not testing a treatment. It may not lead directly to new therapies, and results may not apply to all patients with Dravet syndrome.

Disclaimer Read more

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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Conditions

The condition(s) this trial relates to.

Dravet syndrome Epilepsies, Myoclonic epilepsy

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Study contacts

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

Locations

  • Robert Debré Hospital

    RECRUITING

    Paris, Ap-hp / DRCI, 75019, France

    Contact Phone: •••-•••-•••• Email: •••••@•••••