About Familial abdominal aortic aneurysm
Familial abdominal aortic aneurysm is a rare disease catalogued by Orphanet (ORPHA:86). It is associated with the COL3A1 gene. 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 Familial abdominal aortic aneurysm trials.
Search ClinicalTrials.gov for "Familial abdominal aortic aneurysm" or filter by Orphanet code ORPHA:86 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 Familial abdominal aortic aneurysm trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Familial abdominal aortic aneurysm. Updated daily.