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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Genotype-Phenotype Correlations in Patients With Alport SyndromeAlport syndrome, Collagen Diseases, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Male Urogenital Diseases, Skin and Connective Tissue Diseases, Urogenital Abnormalities, Urogenital Diseases, connective tissue disorder, hereditary nephritis, kidney disorder, nephritis, urinary system disorderRecruitingNot stated2021-07-01NCT04947813

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Research sitesCityCountryLinked trials
China Xinhua Hospital, Shanghai Jiao Tong University School of Medicine.ShanghaiChina1