About Retinopathy of prematurity
Retinopathy of prematurity is a rare disease catalogued by Orphanet (ORPHA:90050). It is associated with the LRP5, FZD4, NDP 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 Retinopathy of prematurity trials.
Search ClinicalTrials.gov for "Retinopathy of prematurity" or filter by Orphanet code ORPHA:90050 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 Retinopathy of prematurity trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Retinopathy of prematurity. Updated daily.