Pneumococcal Post-Vaccination Titers

Sponsor
National Jewish Health (Other)
Overall Status
Unknown status
CT.gov ID
NCT02726347
Collaborator
(none)
140
1
5
24
5.8

Study Details

Study Description

Brief Summary

The study is looking at the pneumonia vaccine and the immune system response to this vaccine. The information gathered from this study may be important for your doctor to take care of patients with smoking histories, immune deficiency, asthma, Chronic Obstructive Pulmonary Disease (COPD), or elderly patients. It is important that your immune system builds a strong defense to the vaccine so that you are better able to fight a bacterium that can cause pneumonia. Some disease prevent the immune system from building a strong defense and these patients will not benefit from the vaccine.

Condition or Disease Intervention/Treatment Phase
  • Biological: PPV-23
N/A

Detailed Description

One hundred forty subjects will have pre-vaccination titers checked for the 23 serotypes in the PPV-23 vaccine. They will then receive the vaccine. All subjects will be given the vaccination as standard of care. Approximately 4 weeks following immunization, the subjects will have post-vaccination titers checked to the same serotypes checked prior to vaccination.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
140 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Official Title:
Pneumococcal Post-Vaccination Titers
Study Start Date :
Apr 1, 2016
Anticipated Primary Completion Date :
Apr 1, 2018
Anticipated Study Completion Date :
Apr 1, 2018

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Smokers between the ages of 19-80

current smokers between the ages of 19 and 80

Biological: PPV-23
one hundred forty subjects will have pre-vaccination titers checked. All will be given vaccination as standard of care. Approximately 4 weeks later subjects will have post-vaccination titers checked for the same serotypes.
Other Names:
  • polysaccharide pneumococcal vaccine
  • Active Comparator: elderly individuals (over age 50)

    elderly individuals, defined as subjects age 50 years or older, without a history of frequent infections, COPD, or asthma

    Biological: PPV-23
    one hundred forty subjects will have pre-vaccination titers checked. All will be given vaccination as standard of care. Approximately 4 weeks later subjects will have post-vaccination titers checked for the same serotypes.
    Other Names:
  • polysaccharide pneumococcal vaccine
  • Active Comparator: COPD subjects

    COPD subjects between the age of 19 and 80, without history of recurrent bacterial infections.

    Biological: PPV-23
    one hundred forty subjects will have pre-vaccination titers checked. All will be given vaccination as standard of care. Approximately 4 weeks later subjects will have post-vaccination titers checked for the same serotypes.
    Other Names:
  • polysaccharide pneumococcal vaccine
  • Active Comparator: Asthmatics subjects

    Asthmatics between the ages of 19 and 80

    Biological: PPV-23
    one hundred forty subjects will have pre-vaccination titers checked. All will be given vaccination as standard of care. Approximately 4 weeks later subjects will have post-vaccination titers checked for the same serotypes.
    Other Names:
  • polysaccharide pneumococcal vaccine
  • Active Comparator: Subjects with recurrent bacterial infections

    Individuals between the age of 19 and 80 who have a history of frequent bacterial infections and are being evaluated for humoral immunodeficiency

    Biological: PPV-23
    one hundred forty subjects will have pre-vaccination titers checked. All will be given vaccination as standard of care. Approximately 4 weeks later subjects will have post-vaccination titers checked for the same serotypes.
    Other Names:
  • polysaccharide pneumococcal vaccine
  • Outcome Measures

    Primary Outcome Measures

    1. Change from pre-to post-vaccination antibody titer [day one- day of vaccine and one month later]

      Evaluate the immune response in the 5 groups of subjects

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    19 Years to 80 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:

    Informed consent will be administered to individuals from 5 cohorts each with 28 subjects for a total of 140 subjects. The cohorts will be:

    1. smokers between the ages of 19-80.

    2. elderly individuals, defined as subjects age 50 years or older, without a history of frequent infections, COPD or asthma.

    3. COPD subjects between the age of 19 and 80, without a history of recurrent bacterial infections.

    4. Asthmatics between the ages of 19 and 80, without a history of recurrent bacterial infections.

    5. individuals between the age of 19 and 80 who have a history of frequent bacterial infections and are being evaluated for humoral immunodeficiency.

    Exclusion Criteria:
    The following groups will be excluded:
    1. Subjects who are currently receiving or have ever received immunoglobulin replacement therapy.

    2. subjects who are on immune suppressive agents.

    3. Subjects who are on chronic steroids or have received an intramuscular injection of steroids in the three months prior to enrollment or oral/intravenous steroids within a month of enrollment or two or more prednisone bursts in the past year.

    4. subjects on antiepileptic agents.

    5. Subjects who have received the pneumococcal polysaccharide vaccine, PPV-23 6) Pregnant women

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 National Jewish Health Denver Colorado United States 80206

    Sponsors and Collaborators

    • National Jewish Health

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Flavia Hoyte, Principal Investigator, National Jewish Health
    ClinicalTrials.gov Identifier:
    NCT02726347
    Other Study ID Numbers:
    • HS-2953
    First Posted:
    Apr 1, 2016
    Last Update Posted:
    Sep 14, 2017
    Last Verified:
    Sep 1, 2017

    Study Results

    No Results Posted as of Sep 14, 2017