About Idiopathic achalasia
Idiopathic achalasia is a rare disease catalogued by Orphanet (ORPHA:930). It is associated with the CRLF1, HLA-DQA1, HLA-DQB1 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 Idiopathic achalasia trials.
Search ClinicalTrials.gov for "Idiopathic achalasia" or filter by Orphanet code ORPHA:930 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 Idiopathic achalasia trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Idiopathic achalasia. Updated daily.