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Clinical Trials/NCT02535546
NCT02535546CompletedNot Applicable

Characterisation of Isolates of Streptococcus Pneumoniae in Patients With Chronic Obstructive Pulmonary Disease

Beaumont Hospital1 site in 1 country150 target enrollmentStarted: July 2014Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
150
Locations
1
Primary Endpoint
Carriage rate of Streptococcus pneumoniae in patients with COPD over four seasons.

Study Overview

Brief Summary

Patients suffering from chronic obstructive pulmonary disease (COPD) commonly get exacerbations of their illness which have many potential triggers including infection. The most common cause of lung infection/pneumonia is an organism named Streptococcus pneumoniae. In Ireland a 13-valent pneumococcal conjugated vaccine (PCV-13) was recently introduced into the childhood vaccination programme. This study aims to investigate the carriage rate of S. pneumoniae in COPD patients over one year and to determine if isolates of S. pneumoniae found within the COPD population would be covered by the PCV-13 vaccine.

Detailed Description

This study aims to determine the potential contribution of S. pneumoniae to the morbidity of patients with COPD in Ireland and if the PCV-13 has potential for reducing infective exacerbations in this cohort. A group of 150 COPD patients are being monitored at quarterly intervals over one year. At each study visit patients report changes to COPD-related medication, recent hospitalisations and exacerbations and provide a sputum sample (or pharyngeal swab if not possible) which is assessed for the presence of S. pneumoniae.

The specific objectives of the study are:

  1. To monitor the carriage rate of pneumococci in a cohort of Irish patients with COPD during and outside periods of acute exacerbation over a one year period.
  2. To assess the COPD exacerbation rate amongst this group of patients.
  3. To monitor changes in the proportion of patients positive for pneumococci carriage over a full season and to document those patients intermittently or permanently colonised.
  4. To characterise S. pneumoniae isolates carried by COPD patients in terms of their genetic evolution, comparison with strains in other countries, and antimicrobial susceptibility.
  5. To assess the proportion of colonised COPD patients that would be covered by current and future pneumococcal vaccines.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Over 18 years of age.
  • Have a clinical diagnosis of COPD.
  • Have a forced expiratory volume at one second/forced vital capacity (FEV1/FVC) ratio < 80%.

Exclusion Criteria

  • Patients too unwell.

Outcomes

Primary Outcomes

Carriage rate of Streptococcus pneumoniae in patients with COPD over four seasons.

Time Frame: One year.

Patients with COPD are being monitored over a one year period for carriage of S. pneumoniae. Carriage is determined by analysis of sputum or pharyngeal swab samples which are collected from patients at quarterly intervals.

Secondary Outcomes

  • Characterisation of carriage isolates of Streptococcus pneumoniae from COPD patients.(One year.)

Investigators

Sponsor
Beaumont Hospital
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Professor Richard Costello

Professor Richard Costello

Beaumont Hospital

Study Sites (1)

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