Viral Infections in Chronic Obstructive Pulmonary Disease (COPD) Exacerbations
NCT ID: NCT00448604
Last Updated: 2010-11-04
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
86 participants
OBSERVATIONAL
2007-05-31
2009-09-30
Brief Summary
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* to determine the prevalence of respiratory virus infections in COPD patients, during and outside acute exacerbation
* to explore the impact of these viral infections on the outcome of these patients
* to explore the association between blood procalcitonin levels and viral infections in this population.
Detailed Description
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Chronic obstructive pulmonary disease (COPD) is a leading cause of morbidity due to repeated exacerbations. The impact of viral infections during and outside COPD exacerbations is poorly understood and there is only scarce data on the role of new biological markers of infection for the management of COPD exacerbations.
Objectives of the project
The investigators aim to
1. describe the epidemiology of viral infections in patients admitted with an exacerbation of their COPD;
2. explore the evolution of viral infections outside exacerbations;
3. analyze the impact of viral infections on clinical outcomes;
4. explore the role of biological markers (CRP, procalcitonin) for the diagnosis and prognosis of viral infections.
Methods
The investigators will prospectively follow-up 100 patients admitted with an acute exacerbation of their COPD. Virological samples will be obtained at admission and at 3 months, to explore the evolution outside episodes of acute exacerbation. Clinical information will be obtained after one-year follow-up. Samples will be tested by RT-PCR for 15 respiratory viruses. The impact of viral infections and the role of biological markers will be explored using univariate and multivariate Cox proportional hazard models.
Conditions
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Keywords
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Age above 18 years
* We plan to include 100 patients with a complete work-up and follow-up
* Written informed consent will be obtained from every participant
Exclusion Criteria
* Patients unable to give their informed consent due to their clinical condition
* Other obvious cause of dyspnea (pulmonary embolism, acute pulmonary edema, lobar pneumonia)
* Patients suffering from bronchiectasis, asthma, pulmonary fibrosis and mineral dust pneumoconiosis
* Patients with a history of active tuberculosis
* Patients with a history of ischemic cerebral stroke and subsequent deglutition dysfunction
18 Years
ALL
No
Sponsors
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Ligue Pulmonaire Genevoise
OTHER
University Hospital, Geneva
OTHER
Responsible Party
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HUG, Geneva
Principal Investigators
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Olivier T Rutschmann, MD, MPH
Role: PRINCIPAL_INVESTIGATOR
University Hospital, Geneva
Locations
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Geneva University Hospital
Geneva, Canton of Geneva, Switzerland
Countries
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References
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Kherad O, Kaiser L, Bridevaux PO, Sarasin F, Thomas Y, Janssens JP, Rutschmann OT. Upper-respiratory viral infection, biomarkers, and COPD exacerbations. Chest. 2010 Oct;138(4):896-904. doi: 10.1378/chest.09-2225. Epub 2010 Apr 30.
Other Identifiers
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06-257
Identifier Type: -
Identifier Source: org_study_id