drugset / Trial / NCT01474863

Citrulline in Severe Sepsis

NCT01474863

RandomizedSingle-groupTriple-blindPrevention

Summary

This is a randomized, double-blind, placebo-controlled, phase 2 study to evaluate biochemical, clinical, and safety effects of 2 doses of intravenous L-citrulline compared to placebo in patients with severe sepsis at risk for or with acute lung injury. The hypothesis is that intravenous L-citrulline will decreased the development or progression of acute lung injury in patients with severe sepsis compared to placebo.

Timeline

Start
2012-08
Primary completion
2016-03
Completion
2016-03

Drugs

EvaluationDrugModalityDoseRoute
Comparator L-citrulline Other / unclassified 4.5 mg/kg Intravenous
Comparator L-citrulline Other / unclassified 9 mg/kg Intravenous