Tissue oxygenation in severe sepsis.

Completed

• Conditions: Severe sepsis/ delirium; 10004018

• Registration Number: NL-OMON34452
• Lead Sponsor: Diakonessenhuis Utrecht

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 6 May 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 50

Inclusion Criteria

age >=18
severe sepsis( 2 SIRS criteria plus focus of infection) and organ failure
written informed consent
Picco guided resuscitation

Exclusion Criteria

Terminal phase of disease

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Main study parameters/endpoints: Primary endpoints will be delirium and the<br /><br>correlation between SrO2 and SvO2. </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Secondary endpoints will be duration of reversal of sepsis, mortality, duration<br /><br>of ICU stay, duration of hospital admittance and duration of mechanical<br /><br>ventilation.</p><br>