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NCT05966818

Effect of Dapagliflozin in Non-Diabetic Patients With Nephrotic Syndrome.

Status unknown Phase 4 Last updated 1 August 2023
What this trial tests

Phase 4 trial testing Dapagliflozin and Standard therapy (ACEI or ARB). in Nephrotic Syndrome in 90 participants. Status unknown.

Timeline
1 August 2023
Primary endpoint
1 January 2024
1 March 2024

Quick facts

Lead sponsorAin Shams University
PhasePhase 4
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment90
Start date1 August 2023
Primary completion1 January 2024
Estimated completion1 March 2024

Drugs / interventions tested

Conditions studied

Sponsor

Ain Shams University

Who can join

Adults 18 to 60, any sex, with Nephrotic Syndrome. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Dapagliflozin is the first SGLT2 inhibitor to be approved for CKD treatment regardless of diabetes status. Since many etiologies of non-diabetic nephropathy are characterized by intraglomerular hypertension, it was hypothesized that dapagliflozin acutely decreases GFR and proteinuria in patients without diabetes at risk of progressive kidney function loss such as nephrotic patients via a glucose independent hemodynamic mechanism. The aim of the study is to assess the effect of Dapagliflozin on proteinuria and estimated glomerular filtration rate in non-diabetic patients with nephrotic syndrome in order to slow the decline in kidney function and the progression to ESRD and to prevent the complications of nephrotic syndrome like thrombotic diseases, peritonitis, hyperuricemia, and recurrent infections.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Nephrotic Syndrome

Currently open trials in the same condition.

Other Ain Shams University trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05966818.

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