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Evaluating Dynamic Arterial Elastance in Septic Shock Patients. — EaDyn  

Septic Shock Clinical Trial

Official title:
Assessment of the Effectiveness and Safety of Dynamic Arterial Elastance in Weaning Vasopressor Support in Patients With Septic Shock: A Randomized Controlled Clinical Trial at Santa Fé Foundation in Bogotá

Clinical Trial Summary

Assess the effectiveness and safety of using dynamic arterial elastance as a tool for weaning vasopressor support in patients with septic shock, compared to a control group

Clinical Trial Description

An open-label, randomized controlled clinical trial will be conducted with two patient groups. Our hypothesis is that using dynamic arterial elastance (EaDyn) as a tool to guide vasopressor weaning can reduce the duration of vasopressor support. Eligible patients will be randomly assigned to either the EaDyn weaning arm or the mean arterial pressure (MAP) weaning arm in a 1:1 ratio. Blinding of participants and investigators will not be possible due to the study's methodology. The analysis will be conducted on an intention-to-treat basis. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06118775
Study type Interventional
Source Fundación Santa Fe de Bogota
Contact
Status Not yet recruiting
Phase N/A
Start date February 1, 2024
Completion date July 1, 2025
View Details
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