About Paroxysmal extreme pain disorder
Paroxysmal extreme pain disorder is a rare disease catalogued by Orphanet (ORPHA:46348). It is associated with the SCN10A, SCN11A, SCN9A 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 Paroxysmal extreme pain disorder trials.
Search ClinicalTrials.gov for "Paroxysmal extreme pain disorder" or filter by Orphanet code ORPHA:46348 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 Paroxysmal extreme pain disorder trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Paroxysmal extreme pain disorder. Updated daily.