Trials / Completed
CompletedNCT00786305
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
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 40 (actual)
- Sponsor
- Groupe Hospitalier Pitie-Salpetriere · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | ceftazidime and amikacin | Nebulized ceftazidime 15 mg/kg/3h during 8 days and nebulized amikacin 25 mg/kg/day during 3 days |
| DRUG | ceftazidime and amikacin | Intravenous infusion of ceftazidime 30 mg/kg over 30 min followed by continuous infusion 90 mg/kg/day during 8 days and intravenous infusion of amikacin 15 mg/kg/day over 30 min during 3 days |
Timeline
- Start date
- 2004-10-01
- Primary completion
- 2008-09-01
- Completion
- 2008-11-01
- First posted
- 2008-11-06
- Last updated
- 2008-11-06
Locations
1 site across 1 country: France
Source: ClinicalTrials.gov record NCT00786305. Inclusion in this directory is not an endorsement.