Search for Genes Influencing Childhood Absence Epilepsy (CAE) Study
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT00041951|
Recruitment Status : Completed
First Posted : July 22, 2002
Last Update Posted : June 1, 2016
|Condition or disease|
|Childhood Absence Epilepsy Epilepsy Seizures|
A high familial predisposition for epilepsy in patients with childhood absence epilepsy (CAE), also called petit mal epilepsy, suggests underlying genetic causes contributing to the disease. Several areas harboring potential absence epilepsy genes have been identified in the genome.
This study will further narrow down those areas and identify gene(s) involved in the cause of CAE by taking several approaches: 1. Comparing patients with CAE to healthy individuals without epilepsy and 2. Investigating whole families with many members affected with epilepsy).
Participation in this study requires an interview regarding medical and family history and saliva (spit) collection from all available family members of families with many epilepsy cases. For those families without a history of epilepsy, parents and children are asked to provide a small amount of saliva only. Healthy volunteers without epilepsy or a family history of seizures are asked to fill out an anonymous questionnaire and provide a small amount of saliva as well.
Although the study is based at Mount Sinai School of Medicine in New York, all study materials can be sent to your home at no cost to participants or their insurance. For the collection of saliva, special containers are provided and they can be shipped back to Mount Sinai in the pre-paid envelope provided. Study materials can be completed at your convenience.
Results from this study may enable scientists to understand the cause of absence seizures and, perhaps, other types of seizures as well and with this laying the foundation for better diagnosis and treatment of epilepsy patients in the future.
|Study Type :||Observational|
|Actual Enrollment :||185 participants|
|Observational Model:||Case Control|
|Official Title:||Search for Genes Influencing Childhood Absence Epilepsy Study|
|Study Start Date :||December 1998|
|Primary Completion Date :||July 2014|
|Study Completion Date :||July 2014|
U.S. FDA Resources
Both parents and a child with CAE of families without other affected members (trios) or whole families with many members affected with epilepsy.
Healthy individuals without epilepsy and no family history of epilepsy.
- Saliva sample [ Time Frame: at baseline ]
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): NCT00041951
|United States, New York|
|Icahn School of Medicine at Mount Sinai|
|New York, New York, United States, 10029|
|Principal Investigator:||Martina Durner, M.D.||Icahn School of Medicine at Mount Sinai|