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RECRUITING
NCT06110130
PHASE4

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

Sponsor: Washington D.C. Veterans Affairs Medical Center

View on ClinicalTrials.gov

Summary

Primary Objective:To study podocyte specific injury markers in African American Veterans with non-diabetic kidney disease(NDKD), on empagliflozin therapy. Primary Endpoint: 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 Objective: 1. Correlate changes in exosome-based podocyte specific proteins with standardized biomarkers of kidney injury including urine albumin/creatinine ratio (ACR) and estimated GFR. 2. Correlate systemic inflammatory markers (focusing on vascular and endothelial function) that are already established such as interleukins (IL1, IL6, IL-12) , hs-CRP and arterial stiffness measures with urine exosome-based podocyte protein estimation. 3. Correlate urine podocyte-specific protein markers with APOL1 mRNA expression levels in blood mononuclear cells (MNC)

Official title: Effect of Empagliflozin on Podocyte Specific Proteins (Injury Markers) in African American Veterans With Non-Diabetic Chronic Kidney Disease

Key Details

Gender

All

Age Range

19 Years - 90 Years

Study Type

INTERVENTIONAL

Enrollment

60

Start Date

2024-02-02

Completion Date

2028-12-01

Last Updated

2025-07-20

Healthy Volunteers

No

Interventions

DRUG

Empagliflozin 10 MG

Take Empagliflozin 10 mg orally daily for 4 months

DRUG

Placebo

Take Placebo 10 mg orally daily for 4 months

Locations (1)

Washington DC Veterans Affairs Medical Center (688)

Washington D.C., District of Columbia, United States