Cerebral Antibiotics Distribution After Acute Brain Injury
NCT ID: NCT01059890
Last Updated: 2016-10-11
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
PHASE1
18 participants
INTERVENTIONAL
2009-09-30
Brief Summary
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Detailed Description
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Conditions
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Study Groups
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Cefotaxime
cefotaxime
Metrodinazole
Metronidazole
Ciprofloxacine
Ciprofloxacin
Fosfocine
Fosfocine
Interventions
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cefotaxime
Metronidazole
Ciprofloxacin
Fosfocine
Eligibility Criteria
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Inclusion Criteria
* Patient who receive an antibiotic for an infection or prophylaxy
* Glasgow coma score \< 8
Exclusion Criteria
* Pregnant woman
* HCV, HIV, HBV infection
18 Years
ALL
No
Sponsors
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Poitiers University Hospital
OTHER
Locations
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Poitiers University Hospital - 2 rue de la Milétrie - Réanimation chirugicale
Poitiers, , France
Countries
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Other Identifiers
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A-BRAIN
Identifier Type: -
Identifier Source: org_study_id
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