Clin2
NCT00478712Likely a fitRecruiting

Genetic study of Hirschsprung disease and family members

Hirschsprung Disease

Part of Digestive system, Genetic & congenital clinical trials.

This study looks at genes in people with Hirschsprung disease and in their first-degree relatives (parents, siblings, and children). It may help researchers understand why Hirschsprung disease happens and how it can vary between families.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
3,000 people
Ages
1 week to 100 years
Study type
Observational

Who can take part

  • You (or the person) have been diagnosed with Hirschsprung disease
  • You may qualify if you are a first-degree relative (parent, sibling, or child) of someone with Hirschsprung disease
  • You must be willing to provide a sample for genetic testing
  • You (or your parent/guardian) must understand the study and agree to consent

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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