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Study identifier: NCT06430684 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Feasibility Trial of Sodium-GLucose coTransporter 2 INhibitors in Pediatric Chronic KIDney DiSease

Condition: Chronic Kidney Diseases · Pediatric Kidney Disease  ·  Sponsor: Ann & Robert H Lurie Children's Hospital of Chicago

PhaseEARLY_Phase 1
Planned participants40
Who can joinAll sexes, 12 Years to 25 Years
Healthy volunteersNo

About this study

The goal of this study is to learn if a clinical trial of sodium-glucose co-transporter 2 inhibitors (SGLT2i) is possible in youth with chronic kidney disease (CKD). The investigators also plan to explore whether treatment with SGLT2i (Empagliflozin) helps improve risk factors for worsening kidney and heart disease. The main questions are: 1. Is enrolling 40 youth with CKD into a clinical trial of empagliflozin feasible (ie achievable)? 2. Does taking empagliflozin for 3 months result in positive changes in blood, urine, and heart function tests? Participants will be randomly selected (like flipping a coin) to either receive empagliflozin or not start treatment with empagliflozin and remain on their usual care. Study Procedures Include * For participants randomly selected for treatment, take empagliflozin once daily for 3 months * Phone calls with researchers every 2 weeks for check-ins * For participants taking empagliflozin, clinic visits 4 and 8 weeks after starting for check-ups and tests * All study participants will have clinic visits at the beginning and end (3 months) where researchers will collect information about their health and perform tests

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

Talk to the study team

Alexander J Kula, MD, MHS  ·  312-227-6160  ·  alexkula@luriechildrens.org

Always discuss trial participation with your own doctor first.

Locations (1)

Ann & Robert H. Lurie Children's Hospital of ChicagoChicago, Illinois, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06430684