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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
ARPKD Database StudyAbnormalities, Multiple, Agenesis of Cerebellar Vermis, Bardet-Biedl syndrome, Caroli disease, Ciliopathies, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Abnormalities, Digestive System Diseases, Eye Diseases, Hereditary, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Male Urogenital Diseases, Meckel syndrome, type 1, Polycystic Kidney, Autosomal Recessive, Urogenital Diseases, bile duct cyst, bile duct disorder, biliary tract disorder, brain disorder, central nervous system disorder, cystic kidney disease, eye disorder, hereditary disease, hypothalamic disorder, isolated congenital hepatic fibrosis, kidney disorder, nephronophthisis, nephronophthisis 1, nervous system disorder, polycystic kidney disease, retinitis pigmentosa, urinary system disorderRecruitingNot stated2026-06-15NCT01401998
Quality of Pediatric Resuscitation in a Multicenter CollaborativeCardiopulmonary Arrest, cardiac arrest, cardiovascular disorder, heart disorderRecruitingNot stated2025-10-02NCT02708134
Growth Trial: Study of the Renata Minima StentArterial Occlusive Diseases, Cardiovascular Abnormalities, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Stenosis, Pulmonary Artery, aorta coarctation, cardiovascular disorder, congenital heart disease, heart disorder, vascular disorderActive, not recruitingNot applicable2025-03-25NCT05086016