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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Genetics in the Progression of NephropathiesAbnormalities, Multiple, Bone Diseases, Metabolic, Chronic Disease, Ciliopathies, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Hemic and Lymphatic Diseases, Male Urogenital Diseases, Neoplasms by Site, Nutritional and Metabolic Diseases, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Urogenital Diseases, acute kidney injury, autosomal dominant polycystic kidney disease, bone disorder, calcium metabolic disease, cardiovascular disorder, chronic renal failure syndrome, cystic kidney disease, endocrine system disorder, hematologic disorder, hematopoietic and lymphoid system neoplasm, hereditary disease, hyperparathyroidism, hypertensive disorder, kidney disorder, kidney failure, metabolic disease, musculoskeletal system disorder, neoplasm, nutritional deficiency disease, nutritional disorder, parathyroid gland disorder, polycystic kidney disease, renal osteodystrophy, rickets, secondary hyperparathyroidism, urinary system disorder, vascular disorder, vitamin D deficiency, vitamin deficiency disorderRecruitingNot stated2024-05-16NCT06416761

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OrganizationsLinked trials
Ospedale San Raffaele19

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Research sitesCityCountryLinked trials
IRCCS Ospedale San RaffaeleMilanItaly85