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临床试验/NCT03848104
NCT03848104已完成不适用

Evaluation of the Use of Cefoxitin in Combination in Continuous Parenteral Administration in the Treatment of Bone and Joint Infections

Hospices Civils de Lyon1 个研究点 分布在 1 个国家目标入组 35 人开始时间: 2018年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
35
试验地点
1
主要终点
Rate of Treatment Failure

研究概览

简要总结

Cephamycin related to 2nd generation cephalosporins, the use of cefoxitin has long been limited to antibiotic prophylaxis. Because of its spectrum (sensitive staphylococci, enterobacteria including ESBL, streptococci, anaerobes), its stability and its low cost, it could be useful in curative bone and joint infections, especially in case of infection polymicrobial disease in patients for whom antibiotic alternative per os is limited.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 100 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • patients havind had a bon and joint infeciton treated with cefoxitin in combination in continuous parenteral administration

排除标准

  • 未提供

结局指标

主要结局

Rate of Treatment Failure

时间窗: Outcome is measured at the end of follow-up (usually between 12 and 24 months after antibiotic therapy disruption

Treatment failure is defined by local clinical and/or microbiological relapse; and/or need for additional surgery; death of septic origin

次要结局

  • Rate of use of this strategy(Outcome is measured at the end of follow-up (usually between 12 and 24 months after antibiotic therapy disruption)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Eugénie MABRUT

clinical research assistant

Hospices Civils de Lyon

研究点 (1)

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