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Rutgers University Study of the Genetics of Kidney Disease

The Rutgers University Study of the Genetics of Kidney Disease

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07217535
Acronym
rugcc-kd
Enrollment
50000
Registered
2025-10-16
Start date
2026-04-23
Completion date
2028-10-31
Last updated
2026-04-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Kidney Disease, Kidney Disease, Chronic, Kidney Disease, End-Stage, Kidney Diseases, Kidney Diseases, Chronic, Kidney Diseases,Cystic

Brief summary

The goal of this observational study is to learn more about how genes impact the risk of kidney disease. Anyone 18 or older living in the US is eligible, and a diagnosis of kidney disease is NOT required. Study participation is online, and it takes about 20 minutes to complete health surveys and request a saliva collection kit sent through US mail. In return, study participants may opt to receive information about their genetic ancestry at no cost.

Detailed description

This is an online research study to learn more about how genes affect the risk of kidney disease. This is an online research study to learn more about how genes affect the risk of kidney disease. No office visit is required and in return, participants may receive information about their genetic ancestry for free. One in seven individuals in the United States today has chronic kidney disease (CDC 2023). The heritability -a measure of genetic, as opposed to environmental, contribution to a disease- of kidney function such as the estimated glomerular filtration rate (eGFR) has been estimated at 38%This study will increase our understanding of the genetic basis of kidney disease, which is a crucial step in drug development to improve current treatment options. The study investigators seek a diverse population because diversity among participants maximizes the usefulness of the data. Participants will use our online study portal to answer questions about their health and provide their DNA via a saliva sample using a pre-paid mailer. Participation takes approximately 20 minutes. Participants will be invited to share data from their electronic health records, but this is not required for study participation. The study investigators keep participants engaged with short monthly newsletters.

Interventions

GENETICSaliva sample

Saliva sample is sent via prepaid US Mail for DNA extraction

Health surveys are filled out online in the study portal.

Sponsors

Rutgers, The State University of New Jersey
Lead SponsorOTHER
Regeneron Pharmaceuticals
CollaboratorINDUSTRY

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* age 18 years or older * currently living in the United States * able to understand and follow written instructions in English * have access to the internet and a computer, laptop, tablet or smart phone * willing to provide written informed consent for participation * willing to provide DNA via a saliva sample using a collection kit mailed to the study participant's home * willing to complete a survey with questions about health related to the study of kidney disease

Exclusion criteria

* Not able to meet or fulfill any of the inclusion criter

Design outcomes

Primary

MeasureTime frameDescription
Genetic risk variants associated with kidney disease2 yearsGenetic factors will be measured through whole exome sequencing along with genotyping of common variants, and then correlated with kidney disease and/or kidney disease subtype.

Countries

United States

Contacts

CONTACTTara Matise, Ph.D.
rugcc-kd@rutgers.edu858-445-3125
CONTACTSteve Buyske, Ph.D.
rutgers-kd@rugcc.edu848-445-7680
PRINCIPAL_INVESTIGATORTara Matise, Ph.D.

Rutgers, The State University of New Jersey

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 25, 2026