EUCTR2018-000059-42-FR进行中（未招募）1 期
Comparison of short infusion versus prolonged infusion of ceftolozane-tazobactam among patients with ventilator associated-pneumonia to Pseudomonas aeruginosa in intensive care units - CEFTOREA
CHU DE TOULOUSE0 个研究点目标入组 60 人开始时间: 2018年4月9日最近更新:
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 60
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •Age = 18 years
- •patients with ventilator associated-pneumonia to Pseudomonas aeruginosa
- •patients hospitalized in intensive care units
- •Pseudomonas aeruginosa susceptible to ceftolozane-tazobactam
- •SAPS II (Simplified Acute. Physiological Score II) > 20
- •Expected duration of survival > 7 days
- •Informed consent of the patient or, failing that, the patient’s close or trustworthy person
- •Affiliated to a social security scheme or equivalent
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 40
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 20
排除标准
- •history of allergy to one of the two molecules
- •history of allergy to betalactamines
- •Strain Isolated resistant to Ceftolozane-Tazobactam combination
- •Renal insufficiency with a glomerular filtration rate evaluated by CKD-EPI < 50 ml/min
- •Patient on dialysis or under continuous hemodiafiltration
- •Pregnant or nursing women
- •Patient benefiting from a system of legal protection for adults
研究者
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