Clin2
NCT06380192Possibly a fitRecruiting

Genetic Epilepsy and Development: A Natural History Study

Developmental and Epileptic Encephalopathy

Part of Brain & nervous system, Genetic & congenital clinical trials.

This study looks at how a specific type of epilepsy with developmental challenges progresses over time. By reusing medical records, the researchers hope to learn more without extra hospital visits.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
400 people
Ages
Any age
Study type
Observational

Who can take part

  • Your child must have a condition that causes both developmental delays and seizures.
  • Your child must be enrolled in a social security program or receive benefits from one.
  • Neither you nor your child can say no to your medical records being used for this research.
  • Your child cannot be under any type of legal guardianship.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

Similar studies

Other trials that look related to this one.

NCT07396883Not yet recruiting
New DNA test for severe epilepsy in children

This trial uses a new, more detailed DNA test (long-read sequencing) to find the cause of severe epilepsy with developmental delays in children when standard genetic testing did not provide an answer. It aims to help families understand the genetic basis of their child's condition.

Besançon
NCT02890641Recruiting
Study of brain signals and genes in hard-to-treat epilepsy

This study looks at genetic factors and brain electrical activity in children whose seizures are difficult to control with standard medicines. It also involves exams like MRI and possibly procedures under anesthesia, to better understand seizure causes and help future care.

Paris
NCT06278428Recruiting
Epilepsy in Infants: Genes and Disease Course

This study looks at children with severe epilepsy that starts before age 2. It aims to understand how different gene changes affect the disease and how it progresses over time.

Ho Chi Minh City
NCT07413211Recruiting
Natural history study for genetic epilepsy and developmental delays

This study follows children and adults with genetic conditions that cause severe epilepsy and developmental delays (DEE), including those with MEF2C mutations. It aims to better understand these disorders and prepare for future clinical trials. You or your child can join in person (travel to NYC), virtually (online), or by filling out a registry.

New York, New York
NCT01858285Recruiting
Genetics study for children with epilepsy

This study looks for genetic (inherited DNA) causes of epilepsy in children. It may help your family better understand what could be driving seizures, even if the cause isn’t known yet.

Boston, Massachusetts
NCT07588971Recruiting
Understanding childhood epilepsy outcomes and long-term patterns

This study tracks children with epilepsy to understand how different types progress over time and what factors affect their outcomes. By learning more about your child's epilepsy journey, researchers hope to improve how doctors predict and manage the condition.

Rome

Hear when a new Developmental and Epileptic Encephalopathy trial opens

We’ll email you when one opens — at most once a week, no account needed, unsubscribe anytime.