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Hirschsprung disease (HD) is a rare congenital disorder of the enteric nervous system, affecting approximately 1 in 5,000 live births. It is characterized by the absence of ganglion cells in the dista...
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Lead Sponsor
University Hospital, Angers
NCT06573723 · Rare Diseases, Amyloidosis, and more
NCT00478712 · Hirschsprung Disease
NCT06650683 · Hirschsprung Disease
NCT07343622 · Total Colonic Aganglionosis, Hirschsprung Disease, and more
NCT07156981 · Hirschsprung Disease
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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