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A Global Active Surveillance for Community Acquired Pneumonia

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Pfizer

Status

Completed

Conditions

Community Acquired Pneumonia

Treatments

Procedure: Nasopharyngeal swab
Procedure: urine specimen
Procedure: Blood draw
Procedure: Chest X-ray
Procedure: sputum

Study type

Interventional

Funder types

Industry

Identifiers

NCT00929721
6115A1-4000

Details and patient eligibility

About

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.

Enrollment

5,172 patients

Sex

All

Ages

50+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 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

Exclusion criteria

  • 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).

Trial design

5,172 participants in 1 patient group

Subjects with Community-Acquired Pneumonia
Other group
Description:
Subjects with Community-Acquired Pneumonia
Treatment:
Procedure: sputum
Procedure: Chest X-ray
Procedure: Blood draw
Procedure: urine specimen
Procedure: Nasopharyngeal swab

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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