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临床试验/NCT07155590
NCT07155590进行中(未招募)不适用

Subphenotype- and Complication-guided Adjunctive Fosfomycin Therapy for Staphylococcus Aureus Bacteraemia: Pooled Analysis of Two Randomised Trials

Hospital Universitari de Bellvitge2 个研究点 分布在 1 个国家目标入组 369 人开始时间: 2025年7月21日最近更新:

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
369
试验地点
2
主要终点
All-cause mortality at 60 days

研究概览

简要总结

Staphylococcus aureus bacteraemia (SAB) is a major global cause of sepsis-related mortality. Randomised trials of adjunctive antibiotics, including fosfomycin, have not shown consistent benefit, possibly due to inclusion of unselected SAB populations. The FEN-AUREUS classification enables early risk stratification based on clinical subphenotypes. The investigators aim to validate this framework in a pooled trial cohort and assess whether combining subphenotypes with IDSA-defined complicated SAB could identify patients most likely to benefit from adjunctive fosfomycin. The investigators will conduct a post-hoc analysis of individual-level data from two multicentre randomised trials-BACSARM and SAFO-evaluating fosfomycin in SAB. Participants will be classified using FEN-AUREUS into source phenotypes (A, B and C) and risk subphenotypes (1 = low-risk, 2 = high-risk). Associations between subphenotype, treatment arm, and outcomes (30/60-day mortality, 8-week treatment success) will be assessed using multivariable models. Monte Carlo simulations will explore power by subgroup. FEN-AUREUS subphenotypes combined with complication status have the potential to identify patients with SAB that could likely benefit form combination therapy with fosfomycin.

研究设计

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

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

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

All-cause mortality at 60 days

时间窗: At 60 days from randomisation

All-cause mortality at 60 days after randomisation

次要结局

  • All-cause mortality at 30 days(At 30 days after randomisation)
  • Treatment success at 8 weeks(At 8 weeks after randomisation)

研究者

发起方
Hospital Universitari de Bellvitge
申办方类型
Other
责任方
Principal Investigator
主要研究者

Francesc Escrihuela-Vidal

MD, PhD

Hospital Universitari de Bellvitge

研究点 (2)

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