Rapid brain infection test could slash unnecessary antibiotic use
NCT ID NCT07432113
First seen Jun 27, 2026 · Last updated Aug 21, 2026 · Updated 1 time
Summary
This study looks at whether a quick diagnostic test (BioFire FilmArray) can accurately predict the cause of meningitis or encephalitis in 182 adults. Participants with symptoms like fever, headache, or confusion will have their spinal fluid tested. The goal is to see if the test helps doctors choose the right treatment faster, reduce unnecessary antibiotics, and shorten hospital stays.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 182 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Apr 2026
- Expected to finish
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Oct 2029
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: Patients aged 18 years or older, of any gender. Presence of at least two of the following symptoms: fever, lethargy, altered level of consciousness, seizures, acute focal deficit, signs of meningeal irritation, or headache. Symptoms must have started within the last 30 days. Obligatory presence of pleocytosis (CSF white blood cell count ≥ 5 cells/mm³). Provision of written Informed Consent (TCLE) by the patient or their legal representative. Exclusion Criteria: * Failure to sign the Informed Consent Form. Clinical manifestations lasting more than 30 days. Patients under 18 years of age. Patients who have undergone neurosurgery within 30 days prior to the onset of symptoms (applies to both prospective and control groups).
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Irmandande Santa Casa de Porto Alegre
RECRUITINGPorto Alegre, Rio Grande do Sul, 90020-090, Brazil
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Other studies related to the condition(s) this trial covers.
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- Scientists probe how meningitis vaccines spark immunity