A Study To Examine Serologic Response In Hospitalized Patients Receiving Polyvalent Pneumococcal Vaccine
NCT ID: NCT00955851
Last Updated: 2010-07-30
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
25 participants
OBSERVATIONAL
2009-06-30
2010-07-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Pneumonia patients
The study group will consist of individuals diagnosed with pneumonia and admitted to the Medicine ward under the Pneumonia Core Measure Protocol.
Pre and post vaccination titers
Titers will be obtained pre vaccination and 4 weeks post vaccination
Interventions
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Pre and post vaccination titers
Titers will be obtained pre vaccination and 4 weeks post vaccination
Eligibility Criteria
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Inclusion Criteria
* Diagnosis of pneumonia requiring hospitalization
* Admission to the Medicine Ward under the Pneumonia Core Measure protocol
* Eligible to receive standard of care pneumococcal vaccine by the treating physician
* Able to receive an injection
* Able to provide informed consent
Exclusion Criteria
* Pregnancy
* Receipt of pneumococcal vaccine within the last 5 years
* Prior history of hypersensitivity reaction to the vaccine
* Unable to return for follow-up testing
18 Years
ALL
No
Sponsors
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George Washington University
OTHER
Responsible Party
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George Washington University Medical Faculty Associates
Locations
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George Washington University Hospital
Washington D.C., District of Columbia, United States
Countries
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Other Identifiers
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010902
Identifier Type: -
Identifier Source: org_study_id