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OpenTrials
Completed

NCT Number: NCT00457977

Comparing Two Pneumococcal Vaccines in Adults With Chronic Obstructive Pulmonary Disease

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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Key information

Age range

40 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

University of Alabama at Birmingham, Birmingham, Alabama, United States

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About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosis of Chronic Obstructive Pulmonary Disease (COPD)
  • Post-bronchodilator forced expiratory volume at one second

/forced vital capacity (FEV1/FVC) level less than 70%

  • Ten or more pack-years of smoking
  • Willing to make return visits to the study clinic and accept telephone contact
  • Last pneumococcal vaccination occured at least 5 years prior to study entry

Exclusion criteria

  • Asthma
  • Sensitivity to pneumococcal vaccine
  • Known bleeding disorder, or requires long-term anticoagulation therapy
  • Presence of chronic disease that may impair pneumococcal vaccine response
  • Acute illness requiring antibiotics in the month prior to study entry
  • Medical condition that makes survival for 24 months following study entry unlikely
  • Pregnant

Treatment and study plan

Pneumovax (PPSV23)

Biological

Injection

Other names: 23-valent pneumococcal capsular polysaccharide vaccine, PPSV23, Pneumovax

Prevnar (PCV7)

Biological

Injection

Other names: 7-valent pneumococcal conjugate vaccine, PCV7, Prevnar

Primary outcomes

  1. Serotype Opsonization Titers

    Time frame: Measured at Baseline, Months 1, 12, and 24

    Opsonophagocytosis activity (OPK) serotype specific geometric means

Secondary outcomes

  1. Serotype-specific Immunoglobulin G (IgG) Antibody Levels

    Time frame: Measured at Baseline, Months 1, 12, and 24

    Serotype-specific immunoglobulin G Geometric Mean IgG antibody levels (ug/ml)

Sponsors and collaborators

Lead sponsor

University of Minnesota

Other

Collaborators

  • National Heart, Lung, and Blood Institute (NHLBI)

Registry information

Official study title

Pneumococcal Vaccine Response in COPD

Acronym: PNEUMO

Important dates

Study start
2007
Primary completion
2011
Study completion
2011
First posted
Apr 9, 2007
Registry last updated
May 12, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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