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Esmolol Infusion for Patients With Septic Shock and Persistent Tachycardia — ECASSS-R  

Septic Shock Clinical Trial

Official title:
Esmolol to Control Adrenergic Storm in Septic Shock - Roll-in

Clinical Trial Summary

This is a prospective, single arm, "roll-in" study of esmolol infusion for patients with septic shock with persistent tachycardia after adequate intravenous volume expansion. The study will evaluate the adequacy and efficiency of study protocols for the anticipated, main ECASSS study, which will have a separate entry in clinicaltrials.gov.

Clinical Trial Description

PRIMARY OBJECTIVE:

To evaluate the adequacy and efficiency of study protocols for the anticipated, randomized, controlled ECASSS study. The primary clinical outcome is organ-failure free days at 28 days, with multiple secondary outcomes, including those relevant to function of and compliance with the study protocols. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02841241
Study type Interventional
Source Intermountain Health Care, Inc.
Contact
Status Completed
Phase Phase 2
Start date April 2016
Completion date March 2017
View Details
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