About Central areolar choroidal dystrophy
Central areolar choroidal dystrophy is a rare disease catalogued by Orphanet (ORPHA:75377). It is associated with the GUCA1A, PRPH2, GUCY2D 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 Central areolar choroidal dystrophy trials.
Search ClinicalTrials.gov for "Central areolar choroidal dystrophy" or filter by Orphanet code ORPHA:75377 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 Central areolar choroidal dystrophy trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Central areolar choroidal dystrophy. Updated daily.