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临床试验/NCT00929721
NCT00929721已完成不适用

Global Active Surveillance for Community-Acquired Pneumonia (CAP) in Adults 50 Years and Older

Pfizer1 个研究点 分布在 1 个国家目标入组 5,172 人开始时间: 2009年12月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
Pfizer
入组人数
5,172
试验地点
1
主要终点
Incidence rates of CAP in adults 50 years and older

研究概览

简要总结

This study is an observational surveillance study to identify adults 50 years and older who present to a study healthcare facility with signs and symptoms of Community-Acquired Pneumonia.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
盲法
None

入排标准

年龄范围
50 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Adult subjects 50 years of age or older
  • •Subject must reside in the surveillance area
  • •Subjects who present to a study healthcare facility where the treating physician clinically suspects CAP

排除标准

  • •Any subject who is transferred to a study healthcare facility after already being hospitalized for 48 hours or more at any other in-patient facility (such as a community hospital).
  • •Hospital Acquired pneumonia (ie, develops signs and symptoms of pneumonia after being hospitalized for 48 hours or more).

研究组 & 干预措施

Subjects with Community-Acquired Pneumonia

Other

Subjects with Community-Acquired Pneumonia

干预措施: Blood draw (Procedure)

Subjects with Community-Acquired Pneumonia

Other

Subjects with Community-Acquired Pneumonia

干预措施: Chest X-ray (Procedure)

Subjects with Community-Acquired Pneumonia

Other

Subjects with Community-Acquired Pneumonia

干预措施: urine specimen (Procedure)

Subjects with Community-Acquired Pneumonia

Other

Subjects with Community-Acquired Pneumonia

干预措施: Nasopharyngeal swab (Procedure)

Subjects with Community-Acquired Pneumonia

Other

Subjects with Community-Acquired Pneumonia

干预措施: sputum (Procedure)

结局指标

主要结局

Incidence rates of CAP in adults 50 years and older

时间窗: up to 120 days from enrollment

次要结局

  • Frequency of bacterial agents associated with CAP, Case fatality and incidence rates of CAP number and characteristics of subjects from outpatient clinics, emergency rooms, and hospital in-patient departments(up to 120 days from enrollment)

研究者

发起方
Pfizer
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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