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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

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Research sitesCityCountryLinked trials
Boston Children'sBostonUnited States3
Children's Hospital of PhiladelphiaPhiladelphiaUnited States22
Children's National HospitalWashington D.C.United States100
Cincinnati Children'sCincinnatiUnited States5
EmoryAtlantaUnited States9
University of UtahSalt Lake CityUnited States72