Skip to content

The effect of empagliflozin on proteinuria

The effect of empagliflozin compared with placebo on proteinuria in patients with glomerulonephritis in Isfahan during 2021

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20090127001598N6
Enrollment
72
Registered
2021-11-22
Start date
2021-11-22
Completion date
Unknown
Last updated
2021-11-29

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

Conditions

Glomerulonephritis. Glomerulonephritis

Interventions

Intervention 1: Intervention group: Patients in this group receive 10 mg Empagliflozin tablets (Gloripa brand, Abidi Pharmaceutical Company, Tehran, 8 km of Shahid Lashkari Highway, Abidi Boulevard, N

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Age more than 18 years old Have at least 500 mg of proteinuria in 24-hour urine and glomerulonephritis and Have a stable condition in proteinuria during the last three months Have eGFR=30 mL/min Written consent to participate in the study Do not use empagliflozin before entering the study Absence of recurrent urinary tract infections Pregnant and lactating patients are not entered in the study

Exclusion criteria

Exclusion criteria: Hypersensitivity reaction to empagliflozin Unwillingness to continue cooperating in the study or not referring for further follow-up Drug or dosage of drugs modification that may affect proteinuria (such as ACEI, ARB, aldosterone blockers, CNI, Mycophenolate, non-dihydropyridine calcium channel blockers) Decreased patient's FBS less than 70 mg / dL during the study Recurrent urinary tract infections

Design outcomes

Primary

MeasureTime frame
Proteinuria. Timepoint: Before starting the study and then three months later. Method of measurement: Measurement of protein in the patient's 24-hour urine.

Secondary

MeasureTime frame
Improve kidney function. Timepoint: At the start and at the end of study. Method of measurement: Measurement of serum creatinine and calculation of eGFR.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShahram Taheri

Esfahan University of Medical Sciences

sh_taheri@tahoo.com+98 31 3620 2020

Outcome results

None listed

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