Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 1:25 AM
Ignite Modification Date:
2025-12-25 @ 1:25 AM
NCT ID:
NCT03317093
Eligibility Criteria:
Inclusion Criteria:
* Adult patients (\> 18 years)
* Provision of informed consent prior to any study specific procedures
* Female patients of childbearing potential may be entered if pregnancy testing is negative and the patient agrees to abstain from procreational sexual intercourse or must use double-barrier contraceptive measures for the duration of the study
* Presence of an indwelling external CSF access device (ventriculostomy or lumbar drain)
* Presence of inflamed meninges as a result of documented or suspected meningitis or ventriculitis. Patients with both clinical symptoms (fever, headache, meningismus, and altered mentation) and laboratory parameters (CSF leukocytosis, defined as a CSF white blood cell count \[WBC\] of \>103, elevated CSF protein, defined as CSF protein of \>1g/l, reduced CSF glucose, defined as CSF glucose of \<0.3g/l, or a positive CSF Gram stain or culture) indicative of CNS infection were deemed to have definitive bacterial meningitis/ventriculitis. Inflamed meninges were defined as the presence of \>5 leukocytes/mm3 of CSF.
* Person with antibacterial treatment (including treatment for the current meningitis or ventriculitis)
* Glycemia above 3 mmol/l and below 10 mmol/l
* Natremia below 145 mmol/l
* Capnia below 45 mmHg
* No other patient included within 72 hours from D0 (treatment period) of the previous patient
* Agreement of the scientific committee
Exclusion Criteria:
* Hypersensitivity to MABELIO® (ceftobiprole) or to one of its excipient or another 3rd cephalosporin
* Hypersensitivity to cephalosporin
* Immediate and severe hypersensitivity to β-lactam antimicrobial other than Mabelio and other cephalosporins
* Pregnant or breast feeding women
* Renal insufficiency defined as creatinine clearance \< 50 mL/min
* Patient with creatinine clearance \> 150 mL/min
* Patients with conditions known or suspected to alter pharmacokinetics (i.e., burn or cystic fibrosis patients)
* Refusal to participate
* Person not affiliated to the social security
* Absolute necessity of immediate removing the device
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT03317093
Study Brief:
Protocol Section:
NCT03317093