Intravenous Fluids in Hospitalised Children

Status Completed

Clinical Trial Summary

The main objective of the trial is to evaluate the risk of hypokalemia following administration of a isotonic solution compared to a hypotonic solution in acutely ill hospitalised children, who need intravenous fluid therapy.

Clinical Trial Description

The main objective of the trial is to evaluate the risk of hypokalemia (low plasma potassium concentration) following administration of a Plasmalyte Glucos 50 mg/mL solution compared to a 0.45% saline in 5% dextrose solution in acutely ill hospitalised children, who need intravenous fluid therapy. The secondary objective of the trial is to evaluate the risk of hyponatremia (low plasma sodium concentration) and the risk of hypernatremia (high plasma sodium concentration) following administration of isotonic solution compared to hypotonic solution. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02926989
Study type	Interventional
Source	University of Oulu
Contact
Status	Completed
Phase	Phase 4
Start date	October 3, 2016
Completion date	April 15, 2019

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