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Genetic Mosaicism in Hirschsprung's Disease

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Erasmus University

Status

Unknown

Conditions

Hirschsprung Disease

Study type

Observational

Funder types

Other

Identifiers

NCT01927809
NL42585.078.12

Details and patient eligibility

About

Hirschsprung's disease is a complex genetic disorder. The etiology of this disease is not completely understood. It is characterized by the absence of ganglia (nerve cells) in de distal colon. This impairs bowel relaxation which can lead to bowel disfunction, toxic megacolon, ileus and enterocolitis. So far, several genes have been identified that play a role in Hirschsprung's disease. The precise mechanisms however, remain unclear. This study wants to identify new mutations and hopefully clarify more about the etiology of the disease.

Enrollment

90 estimated patients

Sex

All

Ages

Under 18 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • All children with Hirschsprung's disease that will receive a corrective pull through procedure

Exclusion criteria

  • None

Trial contacts and locations

2

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Central trial contact

Katherine MacKenzie

Data sourced from clinicaltrials.gov

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