Pharmacoeconomic Analysis of First Line Meropenem Versus Standard Antibiotic Treatment in Seriously Infected Secondary Nosocomial Sepsis Syndrome Patients.
NCT ID: NCT00318552
Last Updated: 2017-09-01
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
PHASE4
160 participants
INTERVENTIONAL
2002-01-31
2006-06-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Interventions
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Meropenem
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Pfizer
INDUSTRY
Principal Investigators
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AstraZeneca CRR Central and Eastern Europe, Hungary Medical Director, MD
Role: STUDY_DIRECTOR
AstraZeneca
Locations
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Research Site
Baja, , Hungary
Research Site
Budapest, , Hungary
Research Site
Eger, , Hungary
Research Site
Kecskemét, , Hungary
Research Site
Kistarcsa, , Hungary
Research Site
Miskolc, , Hungary
Research Site
Pécs, , Hungary
Research Site
Siófok, , Hungary
Research Site
Székesfehérvár, , Hungary
Research Site
Szolnok, , Hungary
Research Site
Szombathely, , Hungary
Research Site
Veszprém, , Hungary
Countries
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Other Identifiers
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D9211C09014
Identifier Type: OTHER
Identifier Source: secondary_id
3591/9014
Identifier Type: -
Identifier Source: org_study_id
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