Swipe the table sideways for more columns.

TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Developing a Pipeline to Employ RNA-Seq as a Complementary Diagnostic Tool in Rare DiseasesAbnormalities, Multiple, Ciliopathies, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cytopenia, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Hemic and Lymphatic Diseases, Male Urogenital Diseases, Urogenital Diseases, anemia, atypical hemolytic-uremic syndrome, autosomal dominant polycystic kidney disease, blood platelet disease, cystic kidney disease, glomerulonephritis, hematologic disorder, hemolytic anemia, hemolytic-uremic syndrome, hereditary disease, immune system disorder, kidney disorder, membranoproliferative glomerulonephritis, nephritis, polycystic kidney disease, thrombocytopenia, thrombotic microangiopathy, uremia, urinary system disorderRecruitingNot applicable2026-03-23NCT05996731

1 results · Page 1 of 1

Swipe the table sideways for more columns.

1 results · Page 1 of 1

Swipe the table sideways for more columns.

Research sitesCityCountryLinked trials
Centro di Ricerche Cliniche per le Malattie Rare "Aldo e Cele Daccò"RanicaItaly6