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Genetic Causes of FSGS, Nephrotic Syndrome, or Kidney Failure — FSGS  

End Stage Renal Disease Clinical Trial

Official title:
Molecular and Genetic Analysis of Inherited Kidney Dysfunction

Clinical Trial Summary

The investigators are trying to learn more about the cause of kidney diseases such as Focal Segmental Glomerulosclerosis (FSGS) and Nephrotic syndrome by studying genetics. The investigators are interested in discovering which genes play a role in causing a predisposition to FSGS/NS. The investigators also want to learn why FSGS/NS can run in families. Participation in our study involves a saliva sample and a urine sample that you can give from home. There is no cost to participate. All information is kept private and confidential. The investigators also like to include healthy volunteers (parents, spouses) if interested/available but of course this is completely optional.

Clinical Trial Description

The investigators welcome anyone (with or without a family history) with unexplained, non syndromic FSGS, nephrotic syndrome, or proteinuria to join the study. Participation involves a saliva (or blood if it is preferable) sample and urine sample (if applicable). There is no cost to participate and the study can be done from home in most cases. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02194582
Study type Observational
Source Beth Israel Deaconess Medical Center
Contact
Status Active, not recruiting
Phase
Start date June 1996
Completion date January 2035
View Details
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