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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
TReatment for ImmUne Mediated PathopHysiologyBrain Diseases, Metabolic, Digestive System Diseases, Hepatic Insufficiency, Nutritional and Metabolic Diseases, acute liver failure, brain disorder, central nervous system disorder, hepatic encephalopathy, liver disorder, liver failure, metabolic disease, nervous system disorderActive, not recruitingPhase 22026-08-12NCT04862221
Neuroblastoma Biology StudyNeoplasms by Histologic Type, Neoplasms, Germ Cell and Embryonal, Neoplasms, Nerve Tissue, Neuroectodermal Tumors, Primitive, Neuroectodermal Tumors, Primitive, Peripheral, epithelial neoplasm, neoplasm, neuroblastoma, neuroepithelial neoplasm, primitive neuroectodermal tumorRecruitingNot stated2026-03-23NCT01587300
Checkpoint Inhibition In Pediatric Hepatocellular CarcinomaDigestive System Diseases, Digestive System Neoplasms, Liver Neoplasms, Neoplasms by Histologic Type, Neoplasms by Site, adenocarcinoma, carcinoma, epithelial neoplasm, fibrolamellar hepatocellular carcinoma, hepatocellular carcinoma, liver cancer, liver disorder, neoplasmRecruitingPhase 22026-02-24NCT04134559
Congenital Heart Disease GEnetic NEtwork Study (CHD GENES)Cardiovascular Abnormalities, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, cardiovascular disorder, congenital heart disease, heart disorderActive, not recruitingNot stated2026-01-30NCT01196182
Phenotypic and Genetic Factors in Autism Spectrum Disordersautism, autism spectrum disorder, autism spectrum disorder 1, neurodevelopmental disorder, pervasive developmental disorder, psychiatric disorderActive, not recruitingNot stated2025-12-29NCT00910559
The Pediatric Anesthesia Quality Improvement ProjectAnesthesia; Children; SurgeryRecruitingNot stated2025-05-21NCT00674388
Natural History Study of SCID DisordersCongenital, Hereditary, and Neonatal Diseases and Abnormalities, DNA repair disease, Infant, Newborn, Diseases, Nutritional and Metabolic Diseases, Omenn syndrome, Primary Immunodeficiency Diseases, X-Linked Combined Immunodeficiency Diseases, X-linked disease, hereditary disease, immune system disorder, inborn error of immunity, metabolic disease, reticular dysgenesis, severe combined immunodeficiency, severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiencyEnrolling by invitationNot stated2020-11-10NCT01186913