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Pneumococcal Vaccine Response in COPD
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.
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.
Age
40 - No limit years
Sex
ALL
Healthy Volunteers
Yes
University of Alabama at Birmingham
Birmingham, Alabama, United States
Veteran's Administration Medical Center
Birmingham, Alabama, United States
LA BioMed at Harbor, University of California
Los Angeles, California, United States
University of California San Francisco-Airway Clinical Research Center
San Francisco, California, United States
Denver Health Medical Center
Denver, Colorado, United States
National Jewish Medical and Research Center
Denver, Colorado, United States
Veteran's Administration Medical Center
Denver, Colorado, United States
University of Maryland Hospital
Baltimore, Maryland, United States
Fallon Clinic
Boston, Massachusetts, United States
Brigham and Women's Hospital
Boston, Massachusetts, United States
Start Date
March 1, 2007
Primary Completion Date
May 1, 2011
Completion Date
May 1, 2011
Last Updated
May 12, 2015
181
ACTUAL participants
Pneumovax (PPSV23)
BIOLOGICAL
Prevnar (PCV7)
BIOLOGICAL
Lead Sponsor
University of Minnesota
Collaborators
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT05050591