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Nebulized Ceftazidime and Amikacin in Ventilator Associated Pneumonia

Assessment of Efficiency of Nebulized Ceftazidime and Amikacin in Treatment of Ventilator Associated Pneumonia Caused by Pseudomonas Aeruginosa

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00786305
Enrollment
40
Registered
2008-11-06
Start date
2004-10-31
Completion date
2008-11-30
Last updated
2008-11-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pneumonia

Keywords

Nebulization, ceftazidime, amikacin, pneumonia, Pseudomonas aeruginosa, mechanical ventilation, Ventilator-associated pneumonia, treatment

Brief summary

Pseudomonas aeruginosa is one of the major causative microorganisms of ventilator-associated pneumonia often resistant to antibiotics. In experimental models, nebulization of antibiotics delivers high lung tissue concentrations of antibiotics in infected lungs and increases lung bacterial killing. The aim of the study is to assess the efficiency of nebulized ceftazidime and amikacin in the treatment of pneumonia caused by Pseudomonas aeruginosa in ventilated patients.

Interventions

DRUGceftazidime and amikacin

Nebulized ceftazidime 15 mg/kg/3h during 8 days and nebulized amikacin 25 mg/kg/day during 3 days

Sponsors

Groupe Hospitalier Pitie-Salpetriere
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Male or female \>18 years old, ventilator associated pneumonia caused by pseudomonas aeruginosa * Written informed consent provided by the relatives

Exclusion criteria

* Pseudomonas aeruginosa resistant to ceftazidime and amikacin * Pseudomonas aeruginosa pneumonia associated with other infections requiring intravenous treatment * Severe septic shock and severe hypoxemia * Allergy to ceftazidime or amikacin

Design outcomes

Primary

MeasureTime frame
Bacterial killing14 days

Secondary

MeasureTime frame
Changes of lung aeration8 days

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026