New study paves way for future treatments in rare brain disorder

NCT ID NCT06018519

First seen Jun 27, 2026 · Last updated Jun 27, 2026

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 to measure symptoms, since many standard tests are too hard for these patients. The goal is to prepare for future clinical trials of new treatments.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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

Contacts and locations

Locations

  • Woman, mother and child hospital, Hospices Civils de Lyon

    RECRUITING

    Bron, 69500, France