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Discontinuation Order of Vasopressors in Septic Shock — DOVSS  

Septic Shock Clinical Trial

Official title:
Incidence of Hypotension Based on the Discontinuation Order of Vasopressors in the Management of Septic Shock

Clinical Trial Summary

The purpose of this study is to evaluate the incidence of hypotension based on the discontinuation order of norepinephrine and vasopressin in patients receiving concomitant norepinephrine and vasopressin infusions for the treatment of septic shock.

Clinical Trial Description

There are little data regarding the discontinuation of vasopressors in patients with septic shock. Therefore, the investigators intend to evaluate the incidence of hypotension based on the discontinuation order of norepinephrine and vasopressin in patients receiving concomitant norepinephrine and vasopressin infusions for the treatment of septic shock. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Supportive Care

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01493102
Study type Interventional
Source Samsung Medical Center
Contact
Status Terminated
Phase N/A
Start date December 2011
Completion date December 2013
View Details
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