Prospective, multicenter, observational clinical registry of adult patients with acute infectious meningitis across approximately 30 public and private hospitals in Brazil. The study will include adults, 18 years old and older, with suspected acute infectious meningitis. Data will be collected during hospitalization and post-discharge to evaluate clinical management, treatment and short and long-term outcomes. The study aims to generate real-world evidence on current practices and outcomes to support improvements in national care protocols.
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:
Both sexes, aged ≥ 18 years, meeting one or more of the criteria (A, B or C) below:
--\> Criterion A: Clinical presentation compatible with a suspected case of meningitis or meningococcal disease:
Fever ≥ 37.8 °C (axillary) associated with at least two of the following:
* Severe headache
* Vomiting
* Altered level of consciousness (confusion, drowsiness, irritability)
* Photophobia
* Seizure OR Fever associated with one of the classic signs of meningeal irritation (neck stiffness, Kernig or Brudzinski signs) OR Sudden-onset fever with petechial rash or hemorrhagic suffusions
* Criterion B: Cerebrospinal fluid with leukocytes ≥ 5 cells/mm³ (corrected for red blood cell count at 1:500)
* Criterion C: Confirmed etiological diagnosis of meningitis or meningococcal disease with no more than 48 hours between pathogen confirmation and signature of the informed consent form by the participant or legal representative.
Exclusion criteria
* Refusal to provide consent for the study.
* Presence of a neurological condition, other than meningitis, that accounts for the current clinical picture.
* Clinical, laboratory or radiological evidence of an alternative infectious focus that accounts for the current clinical picture.
* Use of an intraventricular device prior to study inclusion.
* Etiological diagnosis of meningitis or meningococcal disease confirmed more than 48 hours earlier.
Primary outcome measure(s)
Mortality — Day 28 The primary outcome is the incidence of all-cause death
Trial sites (6)
Facility
City
Region
Status
Hospital Universitário Walter Cantídio
Fortaleza
Ceará
Active Not Recruiting
Hospital São Vicente de Paulo
Passo Fundo
Rio Grande do Sul
Recruiting
Hospitalar Moinhos de Vento
Porto Alegre
Rio Grande do Sul
Recruiting
Hospital das Clínicas da Faculdade de Medicina de Ribeirão Preto - USP
Ribeirão Preto
São Paulo
Recruiting
Hospital Municipal Dr Moysés Deutsch - M'Boi Mirim
São Paulo
Brazil
Recruiting
Hospital Santa Marcelina
São Paulo
Brazil
Recruiting
More Hospital Israelita Albert Einstein trials in Brazil
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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