About Isolated congenitally uncorrected transposition of the great arteries
Isolated congenitally uncorrected transposition of the great arteries is a rare disease catalogued by Orphanet (ORPHA:216718). It is associated with the ZIC3, GDF1, MED13L 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 Isolated congenitally uncorrected transposition of the great arteries trials.
Search ClinicalTrials.gov for "Isolated congenitally uncorrected transposition of the great arteries" or filter by Orphanet code ORPHA:216718 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 Isolated congenitally uncorrected transposition of the great arteries trials
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