Epilepsy Phenome/Genome Project
NCT00552045 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 4150
Last updated 2018-11-13
Summary
The purpose of this study is to collect detailed information about the characteristics and genetics of a large number of individuals with epilepsy.
Conditions
- Epilepsy
- Localization-related Epilepsy
- Infantile Spasms
- Lennox-Gastaut Syndrome
- Polymicrogyria
- Periventricular Heterotopias
Sponsors & Collaborators
-
National Institute of Neurological Disorders and Stroke (NINDS)
collaborator NIH -
University of California, San Francisco
lead OTHER
Principal Investigators
-
Daniel Lowenstein, MD · University of California, San Francisco, Department of Neurology
-
Ruben Kuzniecky, MD · New York University, Comprehensive Epilepsy Center
Eligibility
- Min Age
- 4 Weeks
- Max Age
- 60 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2007-11-30
- Primary Completion
- 2013-12-31
- Completion
- 2018-10-31
Countries
- United States
- Argentina
- Australia
Study Locations
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