Pre-hospital treatment of sepsis: reduction in mortality in severe sepsis.

Recruiting

• Conditions: sepsis; 10004018

• Registration Number: NL-OMON38203
• Lead Sponsor: Albert Schweitzer Ziekenhuis

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 11 June 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: 2200

Inclusion Criteria

1) In the history signs of an infection.
2) Two of the following criteria:
- Respitory Rate of > 20/min
- Heart rate of > 90/min
- A body temperature of > 38 degrees celsius or < 36 degrees celsius
3) Lactate in veneus blood higher or equal to 2,5 mmol/lt

Exclusion Criteria

1) Allergy for beta-lactam.
2) Age <18 jr.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>The reduction of mortality in patients with severe sepsis.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Prehospital treatment related to the organism, co-morbidity, co-medications,<br /><br>gender, age.<br /><br><br /><br>Comparison of the intervention group and control group with APACHE/NICE score.</p><br>