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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Analysis of Patients With Autosomal Dominant Polycystic KidneyAbnormalities, Multiple, Ciliopathies, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Male Urogenital Diseases, Urogenital Diseases, autosomal dominant polycystic kidney disease, cystic kidney disease, hereditary disease, kidney disorder, polycystic kidney disease, urinary system disorderRecruitingNot stated2025-01-06NCT06759142

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Research sitesCityCountryLinked trials
IRCCS Azienda Ospedaliero-Universitaria di BolognaBolognaItaly81