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临床试验/NCT07335627
NCT07335627招募中不适用

Clindamycin as Antimicrobial Treatment for Streptococcus Spp. PeRiprosthetic Infection

University Hospital, Strasbourg, France1 个研究点 分布在 1 个国家目标入组 260 人开始时间: 2025年2月21日最近更新:

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
260
试验地点
1
主要终点
Therapeutic success of the medical-surgical strategy

研究概览

简要总结

Clindamycin is an antibiotic with several advantages: high oral bioavailability and good bone and joint penetration. In France, it is a recommended drug for other types of Streptococcus spp. osteoarticular infections and can be used as an alternative to amoxicillin for periprosthetic infections, including when implants are retained.

The hypothesis of this study is that clindamycin is no less effective than other drugs commonly used to treat periprosthetic Streptococcus spp. infections.

The primary objective of this study is to evaluate the success rate of Streptococcus spp. periprosthetic joint infections treated with clindamycin compared to other antibiotic treatments.

研究设计

研究类型
Observational
观察模型
Case Only
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

  • Adult patient (aged 18 years or older) at the time of surgery for infection
  • Probable or proven periprosthetic infection with Streptococcus spp. according to EBJIS diagnostic criteria
  • Patient operated on in one of the associated centers between 2013 and 2024

排除标准

  • Patient who underwent joint resection or amputation
  • Patient who was treated with suppressive antibiotic therapy (defined as antibiotic treatment lasting more than 6 months) which was decided upon prior to surgery

结局指标

主要结局

Therapeutic success of the medical-surgical strategy

时间窗: One year after the end of antibiotic treatment

Therapeutic success of the medical-surgical strategy defined as: patient showing no clinical signs of infection, no need for repeat surgery one year after the end of antibiotic treatment, and no repeat antibiotic treatment.

次要结局

未报告次要终点

研究者

发起方
University Hospital, Strasbourg, France
申办方类型
Other
责任方
Sponsor

研究点 (1)

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