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Vitamin C and Septic Shock

Sepsis Clinical Trial

Official title:
Evaluating Vitamin C in Septic Shock: A Randomized Double Blind Placebo Controlled Trial

Clinical Trial Summary

This is a randomized, double-blind, placebo-controlled clinical trial to compare Vitamin C versus placebo for patients presenting to the ICU with a diagnosis of septic shock.

Clinical Trial Description

This is a multi-site, randomized, double-blind, placebo-controlled trial comparing a regimen of moderate-dose (6000 mg per day) Vitamin C supplementation versus placebo for the treatment of patients presenting to the ICU with septic shock. Both groups will continue to receive all other standard of care measures for septic shock as clinically indicated. Groups will be enrolled and receive study drug/placebo for 4 days (96 hours) or until 24 hours post-last pressor dose, whichever is sooner. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03338569
Study type Interventional
Source University of Minnesota
Contact
Status Completed
Phase Phase 2/Phase 3
Start date December 20, 2017
Completion date August 10, 2020
View Details
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