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临床试验/NCT01819935
NCT01819935已完成不适用

Clinical Outcomes Among a National Veterans Affairs Methicillin Resistant Staphylococcus Aureus (MRSA) Pneumonia Cohort Treated With Linezolid Or Vancomycin

Pfizer0 个研究点目标入组 5,271 人开始时间: 2012年12月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
Pfizer
入组人数
5,271
主要终点
Time to 30-day Mortality

研究概览

简要总结

The purpose of this non-interventional, retrospective study of existing data is to evaluate clinical outcomes related to Methicillin-resistant Staphylococcus aureus hospital based pneumonia by treatment and among subpopulations.

详细描述

All patients meeting inclusion/exclusion criteria from inpatient database from 1/1/02-9/30/10.

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 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • MRSA and pneumonia cases by ICD-9 code identification.
  • Diagnosis included during inpatient stay.
  • Treatment initiation in hospital.

排除标准

  • Death of discharge within 3 days of treatment initiation.
  • Exposure to other treatments with MRSA activity.

研究组 & 干预措施

linezolid (Zyvox)

干预措施: linezolid (Zyvox) (Drug)

Vancomycin

干预措施: vancomycin (Drug)

结局指标

主要结局

Time to 30-day Mortality

时间窗: Baseline (1 January 2001) up to 3559 Days (30 September 2010)

Time to death (all-cause mortality) occurring within 30 days of treatment initiation was reported. Mortality was assessed from admission vital status databases.

次要结局

  • Time to Therapy Change(Baseline (1 January 2001) up to 3559 Days (30 September 2010))
  • Time to Discharge From the Hospital(Baseline (1 January 2001) up to 3559 Days (30 September 2010))
  • Time to Transfer Out From the Intensive Care Unit (ICU)(Baseline (1 January 2001) up to 3559 Days (30 September 2010))
  • Time to Intubation(Baseline (1 January 2001) up to 3559 Days (30 September 2010))
  • Time to 30-day Re-admission(Baseline (1 January 2001) up to 3559 Days (30 September 2010))
  • Time to 30-day Methicillin-Resistant Staphylococcus Aureus (MRSA) Re-infection(Baseline (1 January 2001) up to 3559 Days (30 September 2010))
  • Clinical Success(Baseline (1 January 2001) up to 3559 Days (30 September 2010))

研究者

发起方
Pfizer
申办方类型
Industry
责任方
Sponsor

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