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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Registry for Hirschsprung Disease of the BELAPSCongenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Abnormalities, Digestive System Diseases, Hirschsprung disease, colonic disorder, digestive system disorder, intestinal disorder, megacolonRecruitingNot stated2024-07-01NCT04622410

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OrganizationsLinked trials
Universitaire Ziekenhuizen KU Leuven262

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Research sitesCityCountryLinked trials
UZ LeuvenLeuvenBelgium236