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Utility of Sodium Lactate Infusion During Septic Shock — ULIS1  

Septic Shock Clinical Trial

Official title:
Utility of Sodium Lactate Infusion During Septic Shock: Pilot Study

Clinical Trial Summary

ULIS-1 is an open-label pilot study concerning utility of molar sodium lactate in fluid balance in septic shock patients

Clinical Trial Description

ULIS-1 consists in three arms of treatment during the first 24hrs of septic shock treatment. - normal saline - sodium lactate 2.5ml/kg in 60min then - either 0.25 or 0.5ml/kg/h during 24hrs Main criteria is fluid balance at 48hrs ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03528213
Study type Interventional
Source University Hospital, Lille
Contact Raphaël Favory, MD,PhD
Phone 03 20 44 54 94
Email raphael.favory@chru-lille.fr
Status Recruiting
Phase Phase 2/Phase 3
Start date October 4, 2019
Completion date November 2023
View Details
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