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Clinical Trial Summary

A randomized, placebo-controlled, double-blind clinical trial of effect of allopurinol or febuxostat to prevent contrast induced acute kidney injury (CI-AKI)


Clinical Trial Description

Eligible patients (patients with glomerular filtration rate < 60 ml/min or high riks patients based on Mehran score) that will be undergoing cardiac catheterization/intervention randomly assigned to receive allopurinol 300 mg or febuxostat 80 mg 12 hours before and 12 after 1 exposure of radiocontrast and IV hydration (normal saline 1 ml/kg/hr 12 pre and post radiocontrast exposure) or placebo and hydration.

Exclusion criteria: patients under treatment with allopurinol or febuxostat in the previous seven days, known allergy to allopurinol or febuxostat, patients on renal replacement therapy ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03767322
Study type Interventional
Source Instituto Nacional de Cardiologia Ignacio Chavez
Contact Magdalena Madero, MD
Phone 01 52 55 5573 2911
Email madero.magdalena@gmail.com
Status Not yet recruiting
Phase Phase 2
Start date December 5, 2018
Completion date December 2019

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