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临床试验/NCT03177343
NCT03177343已完成不适用

Pristinamycin in the Treatment of MSSA Bone and Joint Infection

Hospices Civils de Lyon1 个研究点 分布在 1 个国家目标入组 102 人开始时间: 2015年2月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
102
试验地点
1
主要终点
Efficacy of pristinamycin in MSSA bone and joint infection

研究概览

简要总结

Staphylococcus aureus represents the leading pathogen implicated in bone and joint infection (BJI), usually requiring prolonged combination antimicrobial therapy, which may be particularly challenging in the case of MDR bacteria and/or for patients with multiple drug intolerance. In the absence of new well-tolerated oral antistaphylococcal drugs, older antibiotics must be considered, such as the pristinamycin.

However, pristinamycin is not currently licensed for treatment of staphylococcal BJI and lack of clinical data prevents it from being considered as a reliable alternative therapeutic option in current guidelines.

The aim of this study is to evaluate pristinamycin (efficacy and tolerance) in the treatment of MSSA bone and joint infection (BJI).

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • All patients receiving pristinamycin as a part of treatment for an MSSA BJI and followed up between 2001 and 2011 in the infectious diseases department of Hospices Civils de Lyon (HCL)

排除标准

  • Patients with BJI related to diabetic foot or decubitus ulcer

结局指标

主要结局

Efficacy of pristinamycin in MSSA bone and joint infection

时间窗: 80 weeks

Outcome of patients having had pristinamycin is described in this part. The follow up of the patients after termination of antimicrobial treatment is almost 80 weeks. Treatment failure included: persisting infection under appropriate antimicrobial therapy, relapse after interruption of antimicrobial therapy, septic indication for surgical revision \> 5 days after primary surgery, superinfection; and/or death, if related to the BJI or to complication of its management.

次要结局

  • Tolerance of pristinamycin in MSSA bone and joint infection(45 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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