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ACTIVE NOT RECRUITING
NCT07214818
PHASE2/PHASE3

SGLT2 Inhibitors in Adult Primary Nephrotic Syndrome

Sponsor: Mansoura University

View on ClinicalTrials.gov

Summary

This randomized controlled clinical trial aims to evaluate the efficacy and safety of sodium-glucose cotransporter 2 (SGLT2) inhibitors (dapagliflozin and empagliflozin) in adult patients with primary nephrotic syndrome. The study will compare three groups: dapagliflozin plus standard therapy, empagliflozin plus standard therapy, and standard therapy alone. The primary objective is to assess whether SGLT2 inhibitors reduce proteinuria, maintain remission, and prevent relapse. Secondary objectives include evaluating effects on kidney function (eGFR, serum creatinine) and monitoring safety outcomes. Participants will continue their baseline standard care and will be followed for 6 months with regular clinical evaluations, laboratory tests, and adverse event monitoring.

Official title: Efficacy of Sodium-Glucose Cotransporter 2 Inhibitors in Adult Patients With Nephrotic Syndrome: A Randomized Controlled Trial

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

75

Start Date

2025-11-15

Completion Date

2026-09-06

Last Updated

2026-01-21

Healthy Volunteers

No

Interventions

DRUG

Dapagliflozin

Dapagliflozin 10 mg PO once daily for 6 months

DRUG

Empagliflozin

Empagliflozin 10 mg PO once daily for 6 month

OTHER

Standard Therapy

immunosuppressive therapy and renoprotective agents for 6 months

Locations (1)

Urology & Nephrology Center, Mansoura University

Al Mansurah, Dakahlia Governorate, Egypt