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Clinical Trial Summary

We will look for the possible effect of SGLT2i as a single agent to prevent post-contrast Acute Kidney Injury in diabetic kidney disease.


Clinical Trial Description

Population of Study o Group 1 : 1. st group will receive normal saline 10ml/kg over 6 hours before and 6 hours after radiocontrast. o Group 2 : 2. nd group will receive allopurinol 300 mg and linagliptin 5 mg once daily o Group 3 : 3. rd group will receive the SGLT2i empagliflosin 25 mg once daily o Group 4 : 4. thwill receive allopurinol and empagliflosin. Inclusion Criteria : o Age: more than30years, diabetes,diabetic kidney disease,GFR: more than30ml/min/1.73m2 Exclusion Criteria : o Diabetics Patients with GFR less than 30 mL/min/1.73 m2. Sample Size ( number of participants included ) : 800 patients Fayoum University Faculty of Medicine Scientific Research Ethics Committee Methodology in details : The chosen patients will be randomly allocated to 4 equal groups that will receive their prophylaxis for 48 hours before and 48 hours after the radiocontrast administration. Baseline serum creatinine will be obtained 72 hours before the planned intervention and before administration of any protective protocol and follow-up serum creatinine will be obtained 72 hours and 1 week after contrast administration. The first control group will receive normal saline 10ml/kg over 6 hours before and 6 hours after radiocontrast. Saline should be given by infusion pump to guarantee steady rate of infusion. 2nd group will receive allopurinol 300 mg and linagliptin 5 mg once daily. 3rd group will receive the SGLT2i empagliflosin 25 mg once daily, and the 4th will receive allopurinol and empagliflosin. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04853615
Study type Observational
Source Fayoum University
Contact Ahmed A Hammad, MD
Phone +201001574639
Email [email protected]
Status Not yet recruiting
Phase
Start date July 1, 2021
Completion date August 1, 2024