Pre-hospitale sepsis studie.
Recruiting
- Conditions
- sepsisprehospitalpre-hospitalantibioticssepsisprehospitaalpre-hospitaalantibiotica
- Registration Number
- NL-OMON29015
- Lead Sponsor
- Albert Schweitzer hospital
- Brief Summary
/A
- Detailed Description
Not available
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;
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 The reduction of mortality in patients with severe sepsis.
- Secondary Outcome Measures
Name Time Method 1. Prehospital treatment related to the organism, co-morbidity, co-medications, gender, age;<br /><br>2. Comparison of the intervention group and control group with APACHE/NICE score.