About Atrial septal defect, ostium secundum type
Atrial septal defect, ostium secundum type is a rare disease catalogued by Orphanet (ORPHA:99103). It is associated with the ACTC1, GATA4, MYH6 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 Atrial septal defect, ostium secundum type trials.
Search ClinicalTrials.gov for "Atrial septal defect, ostium secundum type" or filter by Orphanet code ORPHA:99103 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 Atrial septal defect, ostium secundum type trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Atrial septal defect, ostium secundum type. Updated daily.