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Study details
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Feasibility Trial of Sodium-Glucose CoTransporter 2 INhibitors in Pediatric Chronic KIDney DiSease

Ann & Robert H Lurie Children's Hospital of Chicago
NCT IDNCT06430684ClinicalTrials.gov data as of Apr 2026
Phase

EARLY_PHASE1

Target enrollment

40

Study length

about 1.8 years

Ages

12–25

Locations

1 site in IL

What this study is about

Researchers are testing if it's possible to enroll children with chronic kidney disease into a clinical trial of empagliflozin. It will also explore whether taking empagliflozin for three months improves blood, urine, and heart function tests.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take Empagliflozin 10 MG

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Standard

How treatment is administered

Treatment Assignment
Randomized (Open Label)

You are randomly assigned, but you will know your treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Drug classes

empagliflozin (SGLT2 inhibitor; increases glucose excretion in urine)

Endpoints

Secondary: Serum N-terminal pro-brain natruetic peptide (NT-proBNP), Systolic Blood Pressure, Urine Albumin to Creatinine Ratio (UACr)

Body systems

Renal