Epilepsy Phenome/Genome Project (EPGP)
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|ClinicalTrials.gov Identifier: NCT00552045|
Recruitment Status : Unknown
Verified January 2014 by University of California, San Francisco.
Recruitment status was: Active, not recruiting
First Posted : November 1, 2007
Last Update Posted : January 16, 2014
|Condition or disease|
|Epilepsy Localization-related Epilepsy Infantile Spasms Lennox-Gastaut Syndrome Polymicrogyria Periventricular Heterotopias|
Epilepsy is one of the most common neurological disorders and is a major public health concern. Approximately 30 percent of people with epilepsy have medically intractable epilepsy, and the medical and social consequences of the disorder are enormous. Treatments developed for epilepsy have largely been experimental rather than based on knowledge of basic mechanisms because the mechanisms are poorly understood.
The Epilepsy Phenome/Genome Project (EPGP) is a large-scale, international, multi-institutional, collaborative research project aimed at advancing the understanding of the genetic basis of the most common forms of epilepsy.
The overall goal of EPGP is to collect detailed, high quality phenotypic (i.e., characteristics of individuals, from the molecular level to the whole person) information on persons with epilepsy and to compare the phenotypic information with genomic information. EPGP will provide a resource that may lead to many discoveries related to the diagnosis and treatment of epilepsy, including the eventual development of new therapies based on a better understanding of causes of the disorder.
|Study Type :||Observational|
|Actual Enrollment :||4150 participants|
|Observational Model:||Case Control|
|Official Title:||Epilepsy Phenome/Genome Project: A Phenotype/Genotype Analysis of Epilepsy|
|Study Start Date :||November 2007|
|Actual Primary Completion Date :||December 2013|
|Estimated Study Completion Date :||April 2014|
individuals with epilepsy
- EPGP will recruit persons with specific forms of epilepsy. DNA will be isolated from participants' blood and genetic variants associated with common forms of epilepsy will be identified. [ Time Frame: over 4.5 years ]
Biospecimen Retention: Samples With DNA
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00552045
Show 25 Study Locations
|Principal Investigator:||Daniel Lowenstein, MD||University of California, San Francisco, Department of Neurology|
|Principal Investigator:||Ruben Kuzniecky, MD||New York University, Comprehensive Epilepsy Center|