About Familial or sporadic hemiplegic migraine
Familial or sporadic hemiplegic migraine is a rare disease catalogued by Orphanet (ORPHA:569). It is associated with the SCN1A, CACNA1A, ATP1A2 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 Familial or sporadic hemiplegic migraine trials.
Search ClinicalTrials.gov for "Familial or sporadic hemiplegic migraine" or filter by Orphanet code ORPHA:569 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 Familial or sporadic hemiplegic migraine trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Familial or sporadic hemiplegic migraine. Updated daily.