跳至主要内容
临床试验/NCT03317093
NCT03317093已完成2 期

Open and Exploratory Trial to Investigate the Pharmacokinetic of Ceftobiprole Medocaril in Patients With CSF Device

Centre Hospitalier Universitaire Dijon1 个研究点 分布在 1 个国家目标入组 5 人开始时间: 2018年3月29日最近更新:
适应症
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
5
试验地点
1
主要终点
Measurement of concentration of ceftobiprole in blood

研究概览

简要总结

Ceftobiprole is a very active new cephalosporin on staphylococci resistant to methicillin (SEMR: Staphylococcus epidermidis Resistant to Meticillin, SAMR: Staphylococcus aureus Resistant to Meticillin) and / or vancomycin; it is also very active on pneumococci resistant to penicillin and / or 3rd generation cephalosporins. This new drug has AMM in nosocomial respiratory infections, Animal work shows the efficacy of ceftobiprole in gram negative bacillus meningeal infections.

The rationale of this study is based on the antibacterial spectrum of ceftobiprole, which would therefore be useful in the treatment of staphylococcal bacterial meningitis resistant patients (SEMR or SAMR) encountered in intensive care and / or neurosurgery and in the treatment of pneumococcal meningitis.

To validate these possibilities, it is necessary to know the concentrations of ceftobiprole in the meningeal space.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •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

排除标准

  • •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

结局指标

主要结局

Measurement of concentration of ceftobiprole in blood

时间窗: Before and immediately the end of the perfusion and then at 0.5, 1, 3, 6, 12 and 24 hours

Measurement of concentration of ceftobiprole in cerebrospinal fluid

时间窗: Before and immediately the end of the perfusion and then at 0.5, 1, 3, 6, 12 and 24 hours

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验

Open and Exploratory Trial to Investigate the... | 临床试验