Clinical Impact of Fungal Domestic Environmental Exposure on COPD Patients
NCT ID: NCT02318524
Last Updated: 2017-12-22
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
65 participants
OBSERVATIONAL
2011-08-31
2017-10-31
Brief Summary
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As these colonization and sensitization phenomena could be related to domestic exposure to airborne or, for P. jirovecii, to human reservoirs, the investigators set-up a study in order to (i) Evaluate how domestic exposure to mould or to P. jirovecii could impact fungal colonization and sensitization frequency in COPD patients, (ii) Study the relationship between these fungal colonization/sensitization phenomena and lung function impairment in the course of COPD and (iii) Have a better understanding of mould and P. jirovecii circulation in the close environment of patients (between airborne, human reservoirs and patients).
In fine, this study will provide data (i) On fungal contamination levels (species and conidia concentration) of COPD patient's homes in a French region, (ii) On the relationship between fungal exposure level and colonization/sensitization phenomena, (iii) On the role of fungal colonization/sensitization in lung function impairment, (iv) To design diagnostic, therapeutic, and preventive options for the management of COPD patients, taking into account fungal environmental exposure and colonization/sensitization impact on the evolution of the disease.
Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* COPD patient (I to IV stages),
* Medical consultation or severe COPD exacerbation requiring hospitalization.
Exclusion Criteria
* Cancer (or prior anticancer therapy within the past 3 years).
* Diffuse bronchiectasia.
* Cystic fibrosis.
* Asthma.
* Any other pulmonary disease (sarcoidosis, pulmonary fibrosis, pneumoconiosis,…).
* Prior anti- P. jirovecii or antifungal treatment within the past 6 months.
* Pregnant or breast-feeding females.
* Patient with no social insurance.
* Patient unwilling to comply with the protocol.
* Patient unable to understand the study and its objectives.
* Patient under guardianship.
35 Years
90 Years
ALL
No
Sponsors
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Région Nord-Pas de Calais, France
OTHER
Pfizer
INDUSTRY
Merck Sharp & Dohme LLC
INDUSTRY
Gilead Sciences
INDUSTRY
University Hospital, Lille
OTHER
Responsible Party
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Principal Investigators
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Emilie Fréalle, PharmD, PhD
Role: STUDY_DIRECTOR
Lille University Hospital
Stéphanie Fry, MD
Role: PRINCIPAL_INVESTIGATOR
Lille University Hospital
Locations
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Lille University Hospital
Lille, , France
Countries
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Other Identifiers
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2010-A01379-30
Identifier Type: OTHER
Identifier Source: secondary_id
2010_35
Identifier Type: -
Identifier Source: org_study_id