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Clinical Trial Summary

The purpose of this study is to validate a feasible, safe and reliable iohexol plasma clearance method in routine monitoring of the renal function (GFR) in children.

Different parameters of renal function will be compared to the gold standard multiple sample points procedure of iohexol clearance.


Clinical Trial Description

n/a


Study Design

Observational Model: Cohort, Time Perspective: Cross-Sectional


Related Conditions & MeSH terms


NCT number NCT01092260
Study type Observational
Source Haukeland University Hospital
Contact
Status Completed
Phase N/A
Start date April 2010
Completion date December 2011

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