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Bacterial InfectionPhase 1NCT01059890

Cerebral Antibiotics Distribution After Acute Brain Injury

A Phase 1 study testing cefotaxime, Metronidazole and Ciprofloxacin in people with Bacterial Infection and Brain Injury, run by Poitiers University Hospital at 1 site in France.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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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. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Bacterial Infection, Brain Injury
What is being tested?
cefotaxime, Metronidazole and Ciprofloxacin
Could I receive a placebo?
No, everyone receives an active treatment
How many people
18 participants
Where
1 siteFrance
Study dates
Sep 2009to Jun 2013
Phase
Phase 1
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Acute brain injury
  • Patient who receive an antibiotic for an infection or prophylaxy
  • Glasgow coma score < 8

Who cannot join

  • Age < 18 years old
  • Pregnant woman
  • HCV, HIV, HBV infection

Trial locations and contacts

1 site in 1 country.

France1 site
  • Poitiers University Hospital - 2 rue de la Milétrie - Réanimation chirugicale

    Poitiers, 86021

Other trials in France

About this study

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.

Being tested
cefotaxime, Metronidazole, Ciprofloxacin, Fosfocine
Medical subject headings
Bacterial Infections, Brain Injuries

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT01059890
Study groupRoleWhat they receive
CefotaximeExperimentalNot described
Receives: Drug: cefotaxime
MetrodinazoleExperimentalNot described
Receives: Drug: Metronidazole
CiprofloxacineExperimentalNot described
Receives: Drug: Ciprofloxacin
FosfocineExperimentalNot described
Receives: Drug: Fosfocine

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted1 Feb 2010 (estimated)
  2. Study startSep 2009
  3. Primary completionJun 2013

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 1
Enrolment
18 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01059890
Sponsor's protocol ID
A-BRAIN
Status last verified
Oct 2016
First submitted
29 Jan 2010
Last updated
11 Oct 2016
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

A Phase 1 study testing cefotaxime, Metronidazole and Ciprofloxacin in people with Bacterial Infection and Brain Injury, run by Poitiers University Hospital at 1 site in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 11 Oct 2016. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 11 Oct 2016.

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