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The Effect of the Hydroxyethyl Starch on Kidney Injury in Pediatric Cardiac Surgery

Acute Kidney Injury Clinical Trial

Official title:
The Effect of the Hydroxyethyl Starch on Kidney Injury in Pediatric Cardiac Surgery

Clinical Trial Summary

The investigator will evaluate the influence of colloid administration on postoperative acute kidney injury in pediatric patients undergoing cardiac surgery under cardiopulmonary bypass.

Clinical Trial Description

The investigator will randomly divide pediatric patients aged less than 7 years old into crystalloid and colloid groups. Crystalloid group receive only crystalloid, and colloid group receive hydroxyethyl starch (HES, 130/0.4). The maximum volume of HES is limited less than 30 ml/kg. The same transfusion protocol will be applied in both groups. From the day of operation to postoperative 7 days, glomerular filtration rate (GFR), serum creatinin level (Cr) will be checked. Acute kidney injury (AKI) is defined when there is more than 50% increase in Cr when compared to baseline level. The investigator will compare the clinical outcomes including AKI between two groups. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02599155
Study type Interventional
Source Seoul National University Hospital
Contact
Status Completed
Phase N/A
Start date November 2015
Completion date March 2016
View Details
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