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NCT01059890 Clinical Trial

Cerebral Antibiotics Distribution After Acute Brain Injury

Brain Injury Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01059890
Other study ID # A-BRAIN
Secondary ID
Status Completed
Phase Phase 1
First received January 29, 2010
Last updated October 10, 2016
Start date September 2009

Study information
Verified date October 2016
Source Poitiers University Hospital
Contact n/a
Is FDA regulated No
Health authority France: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis)
Study type Interventional

Clinical Trial Summary

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.

Recruitment information / eligibility
Status Completed
Enrollment 18
Est. completion date
Est. primary completion date June 2013
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility 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

Study Design

N/A

Related Conditions & MeSH terms

Intervention

Drug:
• cefotaxime

• Metronidazole

• Ciprofloxacin

• Fosfocine

Locations
Country Name City State
France Poitiers University Hospital - 2 rue de la Milétrie - Réanimation chirugicale Poitiers

Sponsors (1)
Lead Sponsor Collaborator
Poitiers University Hospital

Country where clinical trial is conducted

France, 

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