Severe Septic Shock Complications

Status Not yet recruiting

Clinical Trial Summary

Adults older than 18 years old, admitted to the ICU with a Severe Septic Shock, requiring Norepinephrine at more than 0.25mcg/kg/min, who have signed informed consent form, will be consecutively included, from december 2018 to december 2019.

The primary goal is to look for risk factors associated with an increased in lactate clearance

Secondary goals are the following:

1. To look for risk factors associated with an increase risk of Hospital and ICU length of stay.

2. To look for risk factors associated with an increase risk of Acute Kidney Injury.

3. To look for risk factors associated with a decrease in days alive and free of Mechanical Ventilation, Vasopressors and Renal Replacement Therapy.

4. To look for risk factors associated with a decrease in Ventilator-free days.

5. To look for risk factors associated with a decrease in Vasopressor-free days.

6. To look for risk factors associated with an increase risk of in-hospital mortality.

7. To look for risk factors associated with an increase risk of Myocardial Infarction and myocardial injury.

8. To look for risk factors associated with an increase risk of Acute Respiratory Distress Syndrome.

9. To compare and validate different risk scores in our cohort.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03716895
Study type	Observational [Patient Registry]
Source	Institut d'Investigació Biomèdica de Girona Dr. Josep Trueta
Contact	Marc Vives, PhD, DESA
Phone	+34972940200
Email	marcvives50@gmail.com
Status	Not yet recruiting
Phase
Start date	December 2018
Completion date	March 2020

View Details

See also
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