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Human Epilepsy Genetics--Neuronal Migration Disorders Study

NCT00041600 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 3500

Last updated 2023-09-21

No results posted yet for this study

Summary

The purpose of this study is to identify genes responsible for epilepsy, brain malformations and disorders of human cognition.

Conditions

  • Brain Malformation
  • Neuronal Migration Disorder
  • Cognition Disorder
  • Epilepsy

Sponsors & Collaborators

  • National Institute of Neurological Disorders and Stroke (NINDS)

    collaborator NIH

  • Howard Hughes Medical Institute

    collaborator OTHER

  • Harvard University Faculty of Medicine

    lead OTHER

Principal Investigators

  • Christopher A. Walsh, M.D., Ph.D. · Harvard Institutes of Medicine

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
1996-04-30
Primary Completion
2030-06-30
Completion
2030-06-30

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

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 NCT00041600 on ClinicalTrials.gov