Study Evaluating Antibiotic Use in Reducing Vancomycin-Resistant Enterococci and ESBL Producing Escherichia Coli and Klebsiella Pneumoniae in Intensive Care
NCT ID: NCT00167986
Last Updated: 2007-03-15
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
480 participants
OBSERVATIONAL
2005-01-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Interventions
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vancomycin-resistant enterococci and ESBL
Eligibility Criteria
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Inclusion Criteria
* Patients 18 years of age or older.
* Provide written informed consent.
Exclusion Criteria
* Patients who have hypersensitivity to penicillin.
* Any underlying conditions or diseases that will be ultimately fatal within 48 hours.
* Any concurrent condition or medication which would interfere with absorption or metabolism of study drugs.
18 Years
ALL
No
Sponsors
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Wyeth is now a wholly owned subsidiary of Pfizer
INDUSTRY
Principal Investigators
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Medical Monitor
Role: STUDY_DIRECTOR
Wyeth is now a wholly owned subsidiary of Pfizer
Locations
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Gyunggi-do, , South Korea
Countries
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Other Identifiers
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101498
Identifier Type: -
Identifier Source: org_study_id
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