About Congenital ptosis
Congenital ptosis is a rare disease catalogued by Orphanet (ORPHA:91411). It is associated with the COL25A1, ZFHX4 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 Congenital ptosis trials.
Search ClinicalTrials.gov for "Congenital ptosis" or filter by Orphanet code ORPHA:91411 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 Congenital ptosis trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Congenital ptosis. Updated daily.