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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05062642
Other study ID # CHM-2020/S02/20
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date August 26, 2021
Est. completion date August 26, 2022

Study information

Verified date September 2021
Source Centre Hospitalier le Mans
Contact Christelle JADEAU
Phone 02 44 71 07 81
Email cjadeau@ch-lemans.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Meningitis is the development of an inflammatory reaction in the meningeal space, most often of infectious origin. Many pathogens can cause meningitis, the severity of which varies greatly. Patients presenting with a febrile meningeal syndrome are most often managed in the emergency room, where the challenge for physicians is to quickly differentiate bacterial and viral meningitis. Viral meningitis is the most common, with enterovirus meningitis having a classically excellent prognosis. Bacterial meningitis is less frequent but more serious.The current public health objective is to save antibiotics. Investigator hypothesizes that the BMS score can be used to exclude bacterial meningitis in the emergency department in an adult European population of patients with suspected bacterial meningitis.


Recruitment information / eligibility

Status Recruiting
Enrollment 1000
Est. completion date August 26, 2022
Est. primary completion date August 26, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patient admitted to the Adult Emergency Department of CH Le Mans,CHU Angers, CHU Nantes or Beaujon Hospital. - Over 18 years old - Having had a lumbar puncture during their stay in the Adult Emergency Department - Having had a diagnosis of meningitis defined as a pleocytosis = 5leukocytes/mm3 after correction with CSF red blood cells at a standardized ratio of 500/1. Exclusion Criteria: - Antibiotic therapy within 72 hours of inclusion - Immunosuppression from any cause - Presence of petechiae or purpura - History of recent neurosurgery or head trauma - Other associated bacterial infection - Inability to collect information for the BMS score calculation or primary endpoint (e.g., transfer to another facility) - Minor or adult patient under guardianship or protection

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Centre Hospitalier Du Mans Le Mans

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier le Mans

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary External validation of the BMS score in a European adult population to exclude bacterial meningitis Validation was measured by comparaison between BMS score and the diagnosis retained from the data collected in the file 1 month after inclusion
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