Pneumovax (PPSV23)
BiologicalInjection
Other names: 23-valent pneumococcal capsular polysaccharide vaccine, PPSV23, Pneumovax
NCT Number: NCT00457977
Pneumococcal disease is a serious bacterial infection that can affect different parts of the body, including the lungs. People with chronic illnesses, such as chronic obstructive pulmonary disease (COPD), have a greater risk of developing pneumonia and meningitis as a result of pneumococcal disease. This study will compare the immune response to two types of pneumococcal vaccines in adults with COPD.
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Notify Me40 year and older
All sexes
Interventional
Phase 3
University of Alabama at Birmingham, Birmingham, Alabama, United States
Individuals who are infected with the Streptococcus pneumoniae bacteria may develop pneumococcal disease, a serious disease that kills more people in the United States than all other vaccine-preventable diseases combined. Individuals with COPD, characterized by breathing difficulties due to damaged and obstructed lung airways, may have an increased risk of developing serious complications from pneumococcal disease, including pneumonia and meningitis. Currently, there are two types of pneumococcal vaccines available. The pneumococcal capsular polysaccharide (CPS) vaccine, known as Pneumovax, is typically given to adults 65 years of age or older and to any individuals with a serious health condition, including heart disease, lung disease, and diabetes. The diphtheria protein-conjugated vaccine (PCV7), known as Prevnar, is typically given to infants; however, adults who receive this vaccine may also have a favorable response. The purpose of this study is to compare the immune response to the Pneumovax and Prevnar vaccines in adults with COPD.
This study will enroll adults with mild to moderate COPD. Participants will be randomly assigned to receive either the Pneumovax or Prevnar vaccine. This will involve one or two injections. Blood collection will occur during study visits at Months 1, 12, and 24. Study researchers will contact participants by telephone at Months 6 and 18 to document any pneumococcal infections and any additional pneumococcal vaccinations.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
/forced vital capacity (FEV1/FVC) level less than 70%
Exclusion criteria
Injection
Other names: 23-valent pneumococcal capsular polysaccharide vaccine, PPSV23, Pneumovax
Injection
Other names: 7-valent pneumococcal conjugate vaccine, PCV7, Prevnar
Time frame: Measured at Baseline, Months 1, 12, and 24
Opsonophagocytosis activity (OPK) serotype specific geometric means
Time frame: Measured at Baseline, Months 1, 12, and 24
Serotype-specific immunoglobulin G Geometric Mean IgG antibody levels (ug/ml)
University of Minnesota
Other
Pneumococcal Vaccine Response in COPD
Acronym: PNEUMO
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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