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Genotype-Phenotype Correlations in Patients With Alport Syndrome

Recruitingn/aAges any - anyAllXinhua Hospital, Shanghai Jiao Tong University Sc…
NCT04947813 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

Alport syndrome (AS) is caused by pathogenic variants in the type IV collagen genes COL4A3, COL4A4, and COL4A5. This study aims to enroll families and patients with a history of renal hematuria in 27 hospitals and detect these three genes for AS screening. This study also aims to analysis the effect of COL4A3/COL4A4/COL4A5 genotype on the development of kidney disease.

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📋 Eligibility rules (as published)
Inclusion Criteria: 1. Age: up to 99 Years (Child, Adult, Older Adult) 2. Sex: All; 3. Families and patients with a history of renal hematuria; 4. Those who signed the informed consent. Exclusion Criteria: 1. Polycystic kidney disease, hypertensive nephropathy, etc.; 2. Kidney biopsy is diagnosed as other primary/secondary kidney disease without type IV collagen-related kidney disease, including IgA nephropathy, membranous nephropathy, lupus nephritis, etc. 3. Incomplete medical history or clinical data.
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What it tests

  • Not listed
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Where

1 site
China Xinhua Hospital, Shanghai Jiao Tong University School of Medicine.
Shanghai, China
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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