drugset / Trial / NCT00935168

Crystalloid Versus Hydroxyethyl Starch Trials

NCT00935168

RandomizedParallel-groupQuadruple-blindTreatment

Summary

The aim of this study is to determine whether patients in the Intensive Care Unit who receive fluid resuscitation with either hydroxyethyl starch (a synthetic colloid solution) or saline (a salt solution), have an increased rate of survival at 90 days.

Timeline

Start
2009-12
Primary completion
2012-04
Completion
2012-09

Drugs

EvaluationDrugModalityDoseRoute
Subject hydroxyethyl starch Other / unclassified 50 unknown Intravenous
Comparator sodium chloride Unknown 50 unknown Intravenous

Indications

No indication recorded.