Clinical Trials Directory

Trials / Unknown

UnknownNCT04853615

SGLT2 Inhibitors Prophylaxis Against Post-contrast Acute Kidney Injury in Diabetic Kidney Disease?

Is SGLT2 Inhibitors a Better Prophylactic Agent Against Post-contrast Acute Kidney Injury in Diabetic Kidney Disease? A Multicenter Prospective Randomized Controlled Study

Status
Unknown
Phase
Study type
Observational
Enrollment
800 (estimated)
Sponsor
Fayoum University · Academic / Other
Sex
All
Age
30 Years
Healthy volunteers
Not accepted

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.

Detailed 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.

Conditions

Interventions

TypeNameDescription
DRUGEmpagliflozin 25 MGPAtient will receive empagliflozin 25 mg daily

Timeline

Start date
2021-07-01
Primary completion
2024-07-01
Completion
2024-08-01
First posted
2021-04-21
Last updated
2021-04-26

Regulatory

Source: ClinicalTrials.gov record NCT04853615. Inclusion in this directory is not an endorsement.