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Registry and Natural History of Epilepsy-Dyskinesia Syndromes

NCT06967727 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 700

Last updated 2025-08-17

No results posted yet for this study

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.

Conditions

  • Epilepsy-Dyskinesia
  • Epilepsy
  • Dyskinesia
  • EDS
  • Epilepsy-Dyskinesia Syndomes
  • Epilepsy in Children
  • Dyskinesias
  • Movement Disorders in Children
  • Neurologic Disorder
  • Chorea
  • Myoclonus
  • Ataxia
  • Dystonia Disorder
  • Movement Disorders

Sponsors & Collaborators

Eligibility

Min Age
0 Years
Max Age
30 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-06-01
Primary Completion
2030-06-01
Completion
2030-07-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06967727 on ClinicalTrials.gov