Skip to content
Trial Eligibility
Menu

Effect of Empagliflozin on Podocyte Specific Proteins in African American Veterans With NDKD

NCT06110130

This study is recruiting at 1 US site in 1 state, according to its ClinicalTrials.gov record last updated .

Summary

Primary Objective: To study podocyte specific injury markers in African American Veterans with non-diabetic kidney disease (NDKD), on empagliflozin therapy. Primary Endpoint: We will assess the effect of Empagliflozin on podocyte-specific proteins in exosomes isolated from subjects' urine, such as nephrin, podocalyxin and Wilms'Tumor (WT-1) protein. Secondary Objectives: Correlate changes in exosome-based podocyte specific proteins with standardized biomarkers of kidney injury including urine albumin/creatinine ratio (ACR) and estimated GFR.

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • Chronic Kidney Diseases

Eligibility basics and study details

Study type
Interventional
Phase
Phase 4
Ages
19 to 90 years
Sex
All
Healthy volunteers
Not accepted
Sponsor
Washington D.C. Veterans Affairs Medical Center
Last updated on ClinicalTrials.gov
August 21, 2026

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

District of Columbia · 1

  • Washington DC Veterans Affairs Medical Center (688) · Washington D.C., DC

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.