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The effect of two dosing regimens cefotaxime on the presence of potential pathogenic micro-organisms in airways.

Completed
Conditions
in potential harmful bacteria
potential pathogenic microorganisms
10024970
Registration Number
NL-OMON33091
Lead Sponsor
Medisch Centrum Haaglanden
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
104
Inclusion Criteria

All patients expected to be intubated for more than 24 hours.
All non-intubated patiënts who are expected to receive enteral tube feeding for more than 48 hours.

Exclusion Criteria

Pneumonia at admission on the ICU
Expected death within 48 hours
Immunocompromised patients
Pregnancy
Antibiotic therapy within the last 48 hours before admission at the ICU
No informed consent within 24 hours after admission at the ICU
Cephalosporin allergy
ICU admission in the previous 30 days
Age below 18 years

Study & Design

Study Type
Observational non invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>The primary study parameter is airway colonisation by potential pathogenic<br /><br>microorganisms after four days of selective decontamination of the digestive<br /><br>tract.</p><br>
Secondary Outcome Measures
NameTimeMethod
<p>Secondary study parameters are length of stay on the ICU, length of stay in the<br /><br>hospital, ICU mortality, hospital mortality, duration of mechanical ventilation<br /><br>and pneumonia during ICU admission following the criteria of the Centers for<br /><br>Disease Control.</p><br>
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