Genetics of Rolandic Epilepsy

NCT00282854 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1000

Last updated 2023-06-28

No results posted yet for this study

Summary

The purpose of this study is to find the genes that cause Rolandic epilepsy and its related traits.

Conditions

Sponsors & Collaborators

  • National Institute of Neurological Disorders and Stroke (NINDS)

    collaborator NIH
  • King's College London

    lead OTHER

Principal Investigators

  • Deb K. Pal, MD, PhD · Associate Research Scientist, Mailman School of Public Health, Columbia University Medical Center

Eligibility

Min Age
3 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-01-31
Primary Completion
2013-12-31
Completion
2013-12-31

Countries

  • United States

Study Locations

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Entities

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 NCT00282854 on ClinicalTrials.gov