Epilepsy learning healthcare system registry
Part of Brain & nervous system, Injuries & trauma, Mental health clinical trials.
This is a registry study that collects information from people being treated for epilepsy at participating healthcare centers. The goal is to improve care by learning from real-world patient data.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You are a patient of a healthcare center that is part of the Epilepsy Learning Healthcare System (ELHS).
- You are an established patient there (not just visiting for a second opinion).
- If you have epilepsy, your data will be used for epilepsy-related analyses.
- Even if you don't have epilepsy, you can still be in the registry.
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.
This study collects information about adults who have had an unprovoked seizure or who have epilepsy. The goal is to better understand epilepsy in the community and improve future care.
This is an observational study that looks at how epilepsy is diagnosed and how people do over time, using information from routine care. It may help doctors better understand epilepsy biology and outcomes using real-world data.
This study looks at healthy aging in people with epilepsy. You will fill out a survey to help researchers understand your experiences and needs.
This trial tests a program to help people with epilepsy in Kenya who are not taking their medication regularly get better access to care and support.
This study checks how people with known or suspected epilepsy are evaluated and followed. It may help by improving screening and understanding care for epilepsy in children and adults.
This trial creates a database of health information from people with intellectual disabilities and epilepsy. It aims to help doctors and researchers learn more about these conditions and improve care. The database includes information from medical records, and some people may also be asked to join a research register for future studies.
Hear when a new Epilepsy trial opens
We’ll email you when one opens — at most once a week, no account needed, unsubscribe anytime.