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Trial Match

Clinical trials test new treatments โ€” sometimes the newest options available for a disease. Find trials that are recruiting now, near you. Open one to see its eligibility rules as simple questions to go through with your doctor.

Know your stage or your test results (such as EGFR, HER2 or BRCA)? Match trials to your own profile - nothing you type is saved.

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12 recruiting trials

for Hirschsprung Disease

International Congenital Central Hypoventilation Syndrome (CCHS) Registry and CCHS SHARE NCT03088020n/a1 site๐Ÿ“ Chicago Ilya Khaytin Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford NCT01793168n/a2 sites๐Ÿ“ Sioux Falls๐Ÿ“ Sydney Sanford Health Registry for Hirschsprung Disease of the BELAPS NCT04622410n/a1 site๐Ÿ“ Leuven Universitaire Ziekenhuizen KU Leuven Neurocognition in Congenital Central Hypoventilation Syndrome (CCHS) NCT03568669n/a4 sites๐Ÿ“ Los Angeles๐Ÿ“ Chicago๐Ÿ“ Philadelphia Ilya Khaytin ยท Tests: NIH Toolbox Cognition Battery Long-term Qualitative and Quantitative Outcomes of Children With Hirschsprung's Disease and Anorectal Malformations NCT05450991n/a1 site๐Ÿ“ Liverpool Alder Hey Children's NHS Foundation Trust ยท Tests: Pull through MSOT and MRI for Non-invasive Assessment of Intestinal Transit Time in Children With Chronic Bowel Emptying Disorders NCT06911749NA1 site๐Ÿ“ Erlangen Dr. med. Sonja Diez ยท Tests: MSOT with ICG, MRI Impact of Providing Nursing Support on Parental Stress Related to Preoperative Care of a Newborn with Hirschsprung's Disease NCT06650683NA1 site๐Ÿ“ Marseille Assistance Publique Hopitaux De Marseille ยท Tests: Pediatric HAH Hirschsprung's Advances; Working Towards Autologous tIssue therapIes NCT06590142n/a1 site๐Ÿ“ Liverpool Alder Hey Children's NHS Foundation Trust ยท Tests: Observational study of tissue specimens Institutional Registry of Rare Diseases NCT06573723n/a1 site๐Ÿ“ Buenos Aires Hospital Italiano de Buenos Aires The Influence of Feeding Source on the Gut Microbiome and Time to Full Feeds in Neonates With Congenital Gastrointestinal Pathologies NCT06072976NA1 site๐Ÿ“ Seattle Seattle Children's Hospital ยท Tests: Standard of Care, Exclusive Human Milk Hirschsprung Disease Genetic Study NCT00478712n/a1 site๐Ÿ“ New York NYU Langone Health ยท Tests: Identification of genetic causes of Hirschsprung Disease Improvement of Understanding of Pediatric Sacral Neuromodulation: Therapeutic Strategies and Outcome Variables NCT07519915NA1 site๐Ÿ“ Erlangen Friedrich-Alexander-Universitรคt Erlangen-Nรผrnberg ยท Tests: SNM/MRI/EMG
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