Genetic Studies in Patients and Families With Infantile Spasms
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|ClinicalTrials.gov Identifier: NCT01723787|
Recruitment Status : Active, not recruiting
First Posted : November 8, 2012
Last Update Posted : January 18, 2020
Infantile spasms (IIS), a characteristic epilepsy syndrome of infancy with often catastrophic developmental consequences, is known in some patients to have many different genetic, metabolic and structural etiologies. However, for most patients IIS is the only presenting clinical feature and the specific cause is unknown. Only two FDA approved pharmacologic treatments for IIS exist, Adrenocorticotropic hormone (ACTH) and vigabatrin. While vigabatrin may be the treatment of choice for Tuberous Sclerosis as a cause for IS, ACTH is the treatment of choice for all others. Unfortunately, a substantial number of patients may still not respond to ACTH and there is no a priori way that suggests which patients may be responders. This has led to the following key questions:
Can novel genetic analyses determine known genetic causes of IS with greater efficiency (more timely and cost-effective)? Can novel genetic analyses determine previously unknown disease modifying genes that predispose individuals to develop IS? Can novel genetic analyses elaborate genes and gene polymorphisms that favor ACTH responsiveness? Do these polymorphisms suggest strategies to improve ACTH responsiveness?
|Condition or disease|
Primary Aim 1: Apply whole-exome sequencing to determine possible causes of cryptogenic IS and evaluate adding whole-exome sequencing to standard practice for determining causes of IS. Sub-aim 1: Determine the effectiveness of whole-exome sequencing in suggesting disease-modifying genes that may contribute to triggering IS.
Primary Aim 2: Determine genes, through whole-exome sequencing, that may play a role in determining ACTH responsiveness for IS. Sub-aim 2: Correlate genes or genetic factors (haplotypes) associated with ACTH responsiveness and disease modification.
|Study Type :||Observational|
|Actual Enrollment :||63 participants|
|Official Title:||Genetic Studies in Patients and Families With Infantile Spasms|
|Study Start Date :||March 2013|
|Actual Primary Completion Date :||March 2017|
|Estimated Study Completion Date :||October 2020|
Participants retrospectively identified to have been treated with ACTH according to FDA-approved protocol for Infantile Spasms
Biological parents of participants retrospectively identified to have been treated with ACTH according to FDA-approved protocol for Infantile Spasms
- Determine the effectiveness of novel genetic analyses in suggesting disease-modifying genes that may contribute to triggering IIS. [ Time Frame: Results of the DNA studies will be evaluated prior to completion of the 5th year to assess the need for further investigations. ]Apply novel genetic analyses to determine possible causes of cryptogenic IIS and evaluate adding novel genetic analyses to standard practice for determining causes of IIS
- Determine genes, through novel genetic analyses, that may play a role in determining ACTH responsiveness for IIS [ Time Frame: Results of the DNA studies will be evaluated prior to completion of the 5th year to assess the need for further investigations ]Correlate genes or genetic factors (haplotypes) associated with ACTH responsiveness and disease modification
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): NCT01723787
|United States, Colorado|
|Children's Hospital Colorado|
|Aurora, Colorado, United States, 80045|
|Principal Investigator:||Tim Benke, MD||Children's Hospital Colorado|