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
134 participants
OBSERVATIONAL
2012-10-18
2017-04-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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OTHER
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Normal lung function tests
* Smoker with tobacco consumption of 20 pack/year
* FEV1/FVC\<70% on lung function tests
* no hospitalisation for exacerbation during 3 months before inclusion
* Smoker with tobacco consumption of 20 pack/year
* worsening of pulmonary symptoms
* FEV1/FVC\<70% on lung function tests could be obtain before or 3 months after exacerbation
Exclusion Criteria
* Asthma
* Lung cancer
* Pregnant and lactating women
* Asthma
* Lung cancer
* Pregnant and lactating women
* Asthma
* Lung cancer
* Pregnant and lactating women
50 Years
75 Years
ALL
Yes
Sponsors
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Institut National de la Santé Et de la Recherche Médicale, France
OTHER_GOV
Responsible Party
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Principal Investigators
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Laurent Guilleminault, MD
Role: PRINCIPAL_INVESTIGATOR
Service de Pneumologie, CHRU Tours, Tours, France
Valérie Gissot, MD
Role: PRINCIPAL_INVESTIGATOR
Centre d'Investigation Clinique, CHRU Tours, Tours, France
Antoine Guillon, MD
Role: PRINCIPAL_INVESTIGATOR
Service de Réanimation médicale, CHRU Tours, Tours, France
Locations
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CHRU Tours
Tours, , France
Countries
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Other Identifiers
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2012-A00885-38
Identifier Type: REGISTRY
Identifier Source: secondary_id
C11-56
Identifier Type: -
Identifier Source: org_study_id
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