Plain-English translation of NCT06265103 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
Read our Epilepsy research guide →The Epilepsy Learning Healthcare System (ELHS) is a network study that brings together patients, families, doctors, and researchers to work toward better seizure control and quality of life. Your care information will be collected and shared across the network so that doctors can learn what works best and make faster improvements to epilepsy treatment.
Epilepsy affects millions of Americans, and many people—especially those in underserved communities—face challenges including uncontrolled seizures, depression, and limited access to quality care. This study exists to create a system where real-world data helps doctors quickly identify and spread the most effective practices across all epilepsy centers.
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You will continue your regular epilepsy care at a participating clinic or hospital that is part of the ELHS network. Your medical records and care data will be collected as part of a registry and shared within the network to help improve outcomes. There are no extra visits or procedures required beyond your normal epilepsy appointments.
AI-generated summary from trial data · Jun 4, 2026 · Not medical advice
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