Trials / Completed
CompletedNCT00572559
Microbiologic Response With Linezolid And Vancomycin In Ventilator-Associated Pneumonia Due To Methicillin Resistant Staphylococcus Aureus
A Randomized, Open Label, Multi-Center Clinical Trial, Comparing Microbiologic Response To Linezolid And Vancomycin In Ventilator-Associated Pneumonia (VAP) Due To Methicillin Resistant Staphylococcus Aureus (MRSA)
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 149 (actual)
- Sponsor
- Pfizer · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Ventilator-associated pneumonia (VAP) is a commonplace complication of intensive care patients ventilated for longer than 48 hours. Methicillin-resistant Staphylococcus aureus (MRSA) is the cause of late onset VAP in up to about 30% of cases in US hospitals. Ineffective treatment of MRSA VAP clearly leads to prolonged mechanical ventilation and is probably associated with higher mortality. The purpose of this protocol is to directly compare linezolid and vancomycin specifically for MRSA VAP.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Vancomycin | 1 gram IV every 12 hours for 7 to 14 days |
| DRUG | Linezolid | 600 mg every 12 hours (intravenously \[IV\] for a minimum of the first 4 days followed by a switch to oral if tolerated by patient) for a total duration of 7 to 14 days |
Timeline
- Start date
- 2002-11-01
- Completion
- 2005-01-01
- First posted
- 2007-12-13
- Last updated
- 2010-06-09
Locations
37 sites across 2 countries: United States, Puerto Rico
Source: ClinicalTrials.gov record NCT00572559. Inclusion in this directory is not an endorsement.