Cerebral Antibiotics Distribution After Acute Brain Injury
The recruitment status of this study is unknown because the information has not been verified recently.
Verified January 2010 by Poitiers University Hospital.
Recruitment status was Recruiting
Recruitment status was Recruiting
Sponsor:
Poitiers University Hospital
Information provided by:
Poitiers University Hospital
ClinicalTrials.gov Identifier:
NCT01059890
First received: January 29, 2010
Last updated: NA
Last verified: January 2010
History: No changes posted
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Purpose
The aim of the study is to explore the distribution of antibiotics in the brain after an acute brain injury because brain infections treatment is still an health care problem.
| Condition | Intervention | Phase |
|---|---|---|
|
Bacterial Infection Brain Injury |
Drug: cefotaxime Drug: Metronidazole Drug: Ciprofloxacin Drug: Fosfocine |
Phase 1 |
| Study Type: | Interventional |
Resource links provided by NLM:
Drug Information available for:
Metronidazole
Metronidazole benzoate
Cefoxitin sodium
Cefoxitin
Cefotaxime
Cefotaxime sodium
Metronidazole hydrochloride
Ciprofloxacin
Ciprofloxacin hydrochloride
U.S. FDA Resources
Further study details as provided by Poitiers University Hospital:
| Arms | Assigned Interventions |
|---|---|
| Experimental: Cefotaxime | Drug: cefotaxime |
| Experimental: Metrodinazole | Drug: Metronidazole |
| Experimental: Ciprofloxacine | Drug: Ciprofloxacin |
| Experimental: Fosfocine | Drug: Fosfocine |
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Acute brain injury
- Patient who receive an antibiotic for an infection or prophylaxy
- Glasgow coma score < 8
Exclusion Criteria:
- Age < 18 years old
- Pregnant woman
- HCV, HIV, HBV infection
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01059890
Contacts
| Contact: Claire DAHYOT, MD | 05 49 44 44 44 ext 41369 | c.dahyot-fizelier@chu-poitiers.fr |
Locations
| France | |
| Poitiers University Hospital - 2 rue de la Milétrie - Réanimation chirugicale | Recruiting |
| Poitiers, France, 86021 | |
| Contact: Claire DAHYOT, MD 05 49 44 44 44 ext 41369 c.dahyot-fizelier@chu-poitiers.fr | |
Sponsors and Collaborators
Poitiers University Hospital
More Information
No publications provided
| ClinicalTrials.gov Identifier: | NCT01059890 History of Changes |
| Other Study ID Numbers: | A-BRAIN |
| Study First Received: | January 29, 2010 |
| Last Updated: | January 29, 2010 |
| Health Authority: | France: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis) |
Additional relevant MeSH terms:
|
Bacterial Infections Brain Injuries Brain Diseases Central Nervous System Diseases Nervous System Diseases Craniocerebral Trauma Trauma, Nervous System Wounds and Injuries Cefotaxime Cefoxitin Ciprofloxacin Metronidazole |
Anti-Bacterial Agents Anti-Infective Agents Therapeutic Uses Pharmacologic Actions Nucleic Acid Synthesis Inhibitors Enzyme Inhibitors Molecular Mechanisms of Pharmacological Action Radiation-Sensitizing Agents Physiological Effects of Drugs Antiprotozoal Agents Antiparasitic Agents |
ClinicalTrials.gov processed this record on May 21, 2013