About Self-limited epilepsy with centrotemporal spikes
Self-limited epilepsy with centrotemporal spikes is a rare disease catalogued by Orphanet (ORPHA:1945). It is associated with the GABRG2, GRIN2A, SRPX2 genes. Search below for active recruiting clinical trials from ClinicalTrials.gov, or visit the Orphanet expert page for specialist centres, natural history studies, and patient registries.
Clinical Trial Eligibility Tips
What to know before applying to Self-limited epilepsy with centrotemporal spikes trials.
Search ClinicalTrials.gov for "Self-limited epilepsy with centrotemporal spikes" or filter by Orphanet code ORPHA:1945 to find disease-specific studies.
Ask your specialist to refer you to a Centre of Expertise — Orphanet lists all accredited centres for this condition worldwide.
Natural history studies and patient registries often enrol before drug trials open — contact the Orphanet patient community first.
Patient Resources
Find recruiting Self-limited epilepsy with centrotemporal spikes trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Self-limited epilepsy with centrotemporal spikes. Updated daily.