drugset / Trial / NCT05402397

Losartan and Uric Acid Metabolism in Children With Proteinuric Nephropathies

NCT05402397

Phase 4 Completed 40 enrolled Hospital General de Niños Pedro de Elizalde
RandomizedCrossoverOpen-labelTreatment

Summary

The aim of this study is to assess the serum uric-acid lowering effect of losartan in children with proteinuric nephropathies. Patients already treated with enalapril will be randomized to receive losartan and/or enalapril in a cross-over designed study. Those who recruit the inclusion criteria will receive enalapril and/or losartan during a one month period, followed by a 15 days of wash out (under enalapril treatment). On day 46, the second period of 30 days of treatment start (enalapril or losartan, whichever was not received initially). Before randomization, a baseline 24 hours urine and a fasting blood sample will be obtained to assess uric acid excretion and serum uric acid values along with renal function and electrolyte levels. Then, similar determinations will be performed at days 30, 46 and 76.

Timeline

Start
2022-07-01
Primary completion
2023-12-31
Completion
2024-01-01

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Losartan Other / unclassified 1.4 mg/kg Oral