Nebulized Ceftazidime and Amikacin in Ventilator Associated Pneumonia
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ClinicalTrials.gov Identifier: NCT00786305 |
Recruitment Status :
Completed
First Posted : November 6, 2008
Last Update Posted : November 6, 2008
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
Pneumonia | Drug: ceftazidime and amikacin | Phase 2 |
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 40 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | None (Open Label) |
Primary Purpose: | Treatment |
Official Title: | Assessment of Efficiency of Nebulized Ceftazidime and Amikacin in Treatment of Ventilator Associated Pneumonia Caused by Pseudomonas Aeruginosa |
Study Start Date : | October 2004 |
Actual Primary Completion Date : | September 2008 |
Actual Study Completion Date : | November 2008 |

Arm | Intervention/treatment |
---|---|
Experimental: 1: nebulized ceftazidime and amikacin |
Drug: ceftazidime and amikacin
Nebulized ceftazidime 15 mg/kg/3h during 8 days and nebulized amikacin 25 mg/kg/day during 3 days
Other Name: fortum and amiklin |
Active Comparator: 2: intravenous ceftazidime and amikacin |
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
Other Name: fortum and amiklin |
- Bacterial killing [ Time Frame: 14 days ]
- Changes of lung aeration [ Time Frame: 8 days ]

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Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts 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

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00786305
France | |
Intensive care unit, Department of anesthesiology, La pitie-Salpetriere hospital | |
Paris, France, 75013 |
Principal Investigator: | Jean-Jacques Rouby, MD, PhD | La Pitie-Salpetriere hospital |
Responsible Party: | Jean-Jacques Rouby, Groupe Hospitalier Pitie-Salpetriere |
ClinicalTrials.gov Identifier: | NCT00786305 |
Other Study ID Numbers: |
NATB-2004 |
First Posted: | November 6, 2008 Key Record Dates |
Last Update Posted: | November 6, 2008 |
Last Verified: | November 2008 |
Nebulization ceftazidime amikacin pneumonia |
Pseudomonas aeruginosa mechanical ventilation Ventilator-associated pneumonia treatment |
Pneumonia Pneumonia, Ventilator-Associated Respiratory Tract Infections Infections Lung Diseases Respiratory Tract Diseases Healthcare-Associated Pneumonia Cross Infection |
Iatrogenic Disease Disease Attributes Pathologic Processes Amikacin Ceftazidime Anti-Bacterial Agents Anti-Infective Agents |