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The Efficacy and Safety of Dapagliflozin on Renal Outcomes in Children with Chronic Kidney Disease

The Efficacy and Safety of Dapagliflozin on Renal Outcomes in Children with Chronic Kidney Disease: A Multicenter Randomized Controlled Trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200608047689N4
Enrollment
60
Registered
2025-11-20
Start date
2025-11-21
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Chronic kidney disease, unspecified.. Chronic kidney disease, unspecified.

Interventions

Intervention 1: Intervention group: Children with CKD in the study group will receive dapagliflozin (0.1-0.2 mg/kg) daily in addition to routine treatment for 4 months. Intervention 2: Control group:

Sponsors

Rasht University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to 18 Years

Inclusion criteria

Inclusion criteria: Chronic kidney disease stage 1-4

Exclusion criteria

Exclusion criteria: CKD stage 5 type 1 and type 2 diabetes mellitus Those on renal replacement therapy previous history of allergies to SGLT-2 inhibitors

Design outcomes

Primary

MeasureTime frame
Decreased GFR. Timepoint: Before intervention and 4 months after intervention. Method of measurement: laboratory result.

Secondary

MeasureTime frame
Adverse efffects. Timepoint: Before intervention and 4 months after intervention. Method of measurement: examination.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactElham Bidabadi

Rasht University of Medical Sciences

bidabadi@mail.com+98 13 3372 9104

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Jun 11, 2026