About Congenital short QT syndrome
Congenital short QT syndrome is a rare disease catalogued by Orphanet (ORPHA:51083). It is associated with the SLC4A3, KCNJ2, KCNH2 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 short QT syndrome trials.
Search ClinicalTrials.gov for "Congenital short QT syndrome" or filter by Orphanet code ORPHA:51083 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 short QT syndrome trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Congenital short QT syndrome. Updated daily.