← Eichor
Study identifier: NCT04947813 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Genotype-Phenotype Correlations in Patients With Alport Syndrome

Condition: Alport Syndrome  ·  Sponsor: Xinhua Hospital, Shanghai Jiao Tong University School of Medicine

PhaseN/A
Planned participants8165
Who can joinAll sexes, N/A to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Contact details are listed per location below or on the registry record.

Always discuss trial participation with your own doctor first.

Locations (1)

China Xinhua Hospital, Shanghai Jiao Tong University School of Medicine.Shanghai, ChinaRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT04947813