Clinical Trial

Registry and Natural History of Epilepsy-Dyskinesia Syndromes

Recruiting
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Summary
The Registry and Natural History of Epilepsy-Dyskinesia Syndromes is focused on gathering longitudinal clinical data as well as biological samples (blood, urine, and/or skin/tissue) from male and female patients, of all ages, who have a genetic diagnosis of epilepsy-dyskinesia syndromes. Through prospective review and molecular data analysis, the study aims to identify patterns and correlations between movement and seizure disorders, uncovering genotype-phenotype relationships. The initiative's goals are to enhance understanding of epilepsy-dyskinesia syndromes, inform precision medicine approaches, and foster international collaboration.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2025-05-04.
Status change: Not Yet Recruiting → Recruiting 2025-08-15
Trial Details
NCT Number NCT06967727
Lead Sponsor Boston Children's Hospital
Conditions Epilepsy-Dyskinesia, Epilepsy, Dyskinesia, EDS, Epilepsy-Dyskinesia Syndomes, Epilepsy in Children, Dyskinesias, Movement Disorders in Children +6 more
Enrollment 700 participants
Start Date 2025-06-01
Primary Completion 2030-06-01 (estimated)
Study Completion 2030-07 (estimated)
Updated on ClinicalTrials.gov 2025-08-17