Midodrine Use in Septic Shock

Status Terminated

Clinical Trial Summary

The investigators aim to perform a randomized, double-blind, placebo-controlled trial to investigate the efficacy of midodrine in decreasing time to IV vasopressor liberation in patients with septic shock.

Clinical Trial Description

A growing body of literature comprising largely retrospective data seems to support the safety and efficacy of midodrine in the intensive care unit for decreasing IV vasopressor use. The investigators hypothesize that administration of midodrine in the early phase of septic shock in patients with adequate enteral access will result in a significant decrease in time to IV vasopressor liberation (increase in vasopressor-free days), secondarily resulting in decreased central venous catheter dwell times and intensive care unit length of stay. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03706053
Study type	Interventional
Source	University of Virginia
Contact
Status	Terminated
Phase	Phase 3
Start date	November 5, 2018
Completion date	February 11, 2022

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See also
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