Dissection of Staphylococcus Aureus Infection From Colonization in Cystic Fibrosis Patients (StaphCI)

January 6, 2015 updated by: Barbara Kahl, University Hospital Muenster

Dissection of Staphylococcus Aureus Infection From Colonization in Cystic Fibrosis Patients, a Non-interventional, Prospective, Longitudinal Multicenter Study.

Staphylococcus aureus is not only one of the first pathogens infecting the airways of cystic fibrosis (CF) patients, but also a highly prevalent microorganism (>60% of all CF patients; European and American CF registries; (4,25), which often persists for several years in the respiratory tract of CF patients.

The purpose of this study is to dissect infection by S. aureus from colonization. Therefore, the following non-interventional prospective, longitudinal multicenter study will be conducted to develop the following hypothesis:

CF patients with high bacterial loads are more likely to be infected by S. aureus than patients with low bacterial loads.

Primary endpoint: bacterial load of sputum cultures

Secondary endpoints:

  • nasal carriage
  • molecular analysis of S. aureus (Monoclonal/polyclonal)
  • serum: S. aureus-specific antibodies, S100A12, IL-8, TNF-alpha
  • sputum: S100A12, IL-8, myeloperoxidase
  • S. aureus therapy regimens
  • lung function tests: FEV1, deltaFVC , deltaMEF25
  • BMI development

Inclusion criteria: S. aureus cultures for more than 6 months within the last year, children (>6 years) and patients, who are able to perform lung function tests Exclusion criteria: P. aeruginosa and/or B. cepacia cultures from the specimens for more than 6 months within the last year before recruitment or during the study period In addition to microbiological investigations and clinical laboratory tests, the actual clinical situation will be evaluated and reported during the study period. The results of this observational study will be used to carefully plan a clinical interventional study. Furthermore, with the results it might be possible to characterize a subpopulation of patients, which is at greater risk for S. aureus infections.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Protocol synopsis Title: Dissection of Staphylococcus aureus infection from colonization in cystic fibrosis patients. A non-interventional prospective, 2-year longitudinal multicenter study

Study objectives: The aim of the study is to dissect S. aureus infection from colonization of the pathogen in airway secretions of CF patients during a 2 year period by means of a non-interventional, prospective, longitudinal multicenter study.

The following hypothesis will be developed:

CF patients with high bacterial loads are more likely to be infected by S. aureus than patients with low bacterial loads.

Definition of infection:

  • change in volume, colour or consistency of sputum (exacerbation)
  • increased cough
  • malaise, fatigue or lethargy
  • body temperature more than 38°C
  • new or increased hemoptysis
  • anorexia or weight loss
  • sinus pain or tenderness
  • change in sinus discharge
  • change in chest sounds
  • ten percent decrease in pulmonary function from a previous recorded value (FEV1, MEF25)
  • radiographic changes indicative of pulmonary infection

Primary endpoint: bacterial load of sputum cultures [high (>/= 106CFU/ml); low (<106CFU/ml)]

Secondary endpoints are:

  • assessment of nasal S. aureus carriage
  • serum samples: antibody titres against S. aureus specific antigens; S100A12, IL-8,TNF-alpha, CRP
  • molecular analysis of S. aureus colonization/infection (monoclonal or heteroclonal)
  • sputa analysis: activity of S100A12, IL-8 and myeloperoxidase
  • antibiotic treatment regimens against S. aureus
  • body mass index
  • lung function tests: FEV1, deltaFVC, deltaMEF25

Extensive microbiological investigations will be performed when the patients are seen at their regular visits in the outpatient clinics or if exacerbations occur. During the study period of 2 years, at least 8 visits to the outpatient clinic should be recorded. The following clinical parameters will be documented:

  • lung function
  • body mass index (weight/height)
  • antibiotic treatment Diagnosis: CF and positive S. aureus cultures for more than 6 months within the last year Localisation of the study: multicenter study in Germany Number of centers: Seven centres agreed already to participate in the study. More centers have been and will be contacted.

Design: non-interventional prospective, longitudinal multicenter study Planned number of patients/volunteers: 228 Inclusion criteria: positive S. aureus cultures for more than 6 months within the last year; children (>6 years) and patients with CF, who are able to perform lung function tests Exclusion criteria: Pseudomonas aeruginosa and/or Burkholderia cepacia colonization or infection for more than 6 months within the last year before recruitment; patients who have not been colonized with these pathogens before but acquire them within the study period and are colonized/infected for more than 6 months during the observation period

Study Type

Observational

Enrollment (Actual)

195

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Innsbruck, Austria, 6020
        • Medizinische Universität Innsbruck
      • Berlin, Germany, 12200
        • Charite Berlin Campus Benjamin Franklin
      • Bochum, Germany, 44791
        • Clinic for Children and Adolescents Ruhr University Bochum St Josef Hospital
      • Dresden, Germany, 01307
        • Universitätsklinikum Carl Gustav Carus
      • Duesseldorf, Germany, 40225
        • Heinrich-Heine University Duesseldorf
      • Essen, Germany, 45122
        • University Clinics Essen
      • Essen, Germany, 45239
        • Ruhrlandklinik Essen-Heidhausen
      • Halle, Germany, 06120
        • Universitätsklinikum Halle
      • Hamburg, Germany, 22763
        • Dres Heuer-Runge-Sextro
      • Hannover, Germany, 30625
        • Medical School Hannover
      • Jena, Germany, 07743
        • University Clinics Jena
      • Kassel, Germany, 34121
        • Children's Hospital Park Schoenfeld
      • Leipzig, Germany, 04103
        • Universitätsklinikum Leipzig
      • Muenster, Germany, 48149
        • University Clinics Muenster
      • Muenster, Germany, 48153
        • Clemenshospital
      • Osnabrueck, Germany, 49082
        • Children's Hospital Osnabrueck
      • Tuebingen, Germany, 72076
        • University Clinics Tuebingen

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

6 years and older (Child, Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

CF-patients with persistent S. aureus culture in their airway specimens

Description

Inclusion Criteria:

  • positive S. aureus cultures for more than 6 months within the last year; children (>6 years) and patients with CF, who are able to perform lung function tests

Exclusion Criteria:

  • Pseudomonas aeruginosa and/or Burkholderia cepacia colonization or infection for more than 6 months within the last year before recruitment; patients who have not been colonized with these pathogens before but acquire them within the study period and are colonized/infected for more than 6 months during the observation period

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Observation
CF-patients with persistent culture of Staphylococcus aureus in their respiratory specimens
does not apply
Other Names:
  • does not apply

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
bacterial load of sputum cultures [high (>/= 1000000CFU/ml); low (<1000000CFU/ml)]
Time Frame: 2 years
2 years

Secondary Outcome Measures

Outcome Measure
Time Frame
antibody titres against S. aureus specific antigens; S100A12, IL-8, TNF-alpha, CRP
Time Frame: 2 years
2 years

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Barbara C Kahl, MD, Dept. Med. Microbiology, University Clinics Muenster, Germany

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Helpful Links

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

July 1, 2008

Primary Completion (Actual)

July 1, 2011

Study Completion (Actual)

January 1, 2015

Study Registration Dates

First Submitted

April 28, 2008

First Submitted That Met QC Criteria

April 29, 2008

First Posted (Estimate)

April 30, 2008

Study Record Updates

Last Update Posted (Estimate)

January 7, 2015

Last Update Submitted That Met QC Criteria

January 6, 2015

Last Verified

January 1, 2015

More Information

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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