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A Study To Examine Serologic Response In Hospitalized Patients Receiving Polyvalent Pneumococcal Vaccine

A Study To Examine Serologic Response In Hospitalized Patients Receiving Polyvalent Pneumococcal Vaccine

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00955851
Enrollment
25
Registered
2009-08-10
Start date
2009-06-30
Completion date
2010-07-31
Last updated
2010-07-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pneumonia

Brief summary

Investigators in the Division of Infectious Diseases and the Division of Hospital Medicine of The George Washington University Medical Center are carrying out a study to determine if hospitalized patients receiving the polyvalent pneumococcal vaccine during an acute illness develop an adequate antibody response. The study group will consist of individuals diagnosed with pneumonia and admitted to the Medicine ward under the Pneumonia Core Measure Protocol, which assigns appropriate patients for vaccination based on the current guidelines from the Advisory Committee on Immunization Practices (ACIP).

Interventions

OTHERPre and post vaccination titers

Titers will be obtained pre vaccination and 4 weeks post vaccination

Sponsors

George Washington University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Males or female patients ages 18 or older * 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

* Preexisting history of immunosuppression, to include any of the following: HIV/AIDS, Chronic corticosteroid use, Malignancy requiring myeloablative chemotherapy, Hematologic malignancy, History of solid organ or stem cell transplant * 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

Design outcomes

Primary

MeasureTime frame
A change in the pre- and post-vaccination pneumococcal serotype-specific IgG concentration from baseline will be considered protective based on the laboratory reference range.5 weeks

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026