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Clinical Trial of the Optimal Endpoint of Early Sepsis Resuscitation — LactATES  

Septic Shock Clinical Trial

Official title:
Lactate Assessment in the Treatment of Early Sepsis: The LactATES Trial

Clinical Trial Summary

The purpose of this study is to determine if there is equivalence between two different methods of treating patients with severe bloodstream infection called sepsis. We will randomly assign patients to one of two treatment methods. One of the treatment methods is the current standard of care and uses an infrared sensor on the end of a catheter to determine the adequacy of treatment. The second treatment method is identical to the first but instead of the infrared sensor a blood test that is performed as a part of standard care (with blood drawn from the catheter) will be used to determine the adequacy of treatment. This study will attempt to determine an easier method of guiding treatment.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Bio-equivalence Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00372502
Study type Interventional
Source National Institute of General Medical Sciences (NIGMS)
Contact
Status Completed
Phase N/A
Start date January 2007
Completion date December 2008
View Details
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