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The effect of empagliflozin on proteinuria

A study to assess the safety and tolerability of the SGLT2 inhibitor empagliflozin on proteinuria in non-diabetic patients

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220405054414N1
Enrollment
15
Registered
2023-08-27
Start date
2023-04-30
Completion date
Unknown
Last updated
2023-10-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Proteinuria. Persistent proteinuria, unspecified

Interventions

Intervention group: All non-diabetic proteinuria patients aged 5 to 17 years are first given half a tablet of empagliflozin 10 mg (Gloripa manufactured by Abidi company) for 3 months, and if they tole

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
5 Years to 17 Years

Inclusion criteria

Inclusion criteria: Age between 5 to 17 years old Suffering from non-diabetic proteinuria according to the diagnosis of a nephrologist Receiving a clinically appropriate dose of ACEIs or ARBs unless treatment is not tolerated or indicated GFR more than 60ml/min

Exclusion criteria

Exclusion criteria: Moderate to severe liver failure Having type 1and 2 diabetes Sensitivity to any of the components of the drugs used Hypotension Receiving immunosuppressants in the last 6 months Having Polycystic kidney disease Poor patient compliance during medication visits Kidney transplant Concurrent administration of ACEIs or ARBs

Design outcomes

Primary

MeasureTime frame
Change in body measurement. Timepoint: baseline to 24 weeks. Method of measurement: scales.;Change in blood pressure. Timepoint: baseline to 24 weeks. Method of measurement: Pressure gauge device.;Change in eGFR. Timepoint: baseline to 24 weeks. Method of measurement: schwartz method.;Change in glycemic control. Timepoint: baseline to 24 weeks. Method of measurement: blood draw from vein.;Time to the first occurrence of urinary infection. Timepoint: baseline to 24 weeks. Method of measurement: urine analysis.;Time to first occurrence of AKI. Timepoint: baseline to 24 weeks. Method of measurement: SCr.

Secondary

MeasureTime frame
Change from baseline in proteinuria. Timepoint: Baseline to ?? weeks. Method of measurement: Urin analysis.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammadreza Maghamipour

Iran University of Medical Sciences

mmaghami11@yahoo.com0214460618

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026