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RECRUITINGINTERVENTIONAL

Incident Chronic Obstructive pulmoNary dIsease Cohort Study (ICONIC)

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

Chronic Obstructive Pulmonary Disease (COPD), , secondary to smoking, is a major public health issue with very high direct and indirect costs. The impact on the health system of undiagnosed patients, up to 70% of patients, is increasingly documented. However, systematic spirometry screening remains controversial among smokers in the absence of data to link the detection of new patients with improved management and clinical events and health goals. More generally, there is little data on the evolution of patients in real life once they have entered the care system. The premise is that with systematic screening in general medicine, it is possible to identify the evolution of newly diagnosed COPD patients, to distinguish the different possible evolutions according to the initial phenotype and the management.

Who May Be Eligible (Plain English)

Who May Qualify: Inclusion criteria of smokers with spirometry (pre-inclusion) - Age\> 35 years - Smoking \> 20 PA - Active smoking (cessation \< 1 month) - Signature of consent to participate in Phase I of the study Inclusion criteria for patients with incidental COPD - FEV1 / FVC \<70% of the theoretical value and / or \<LLN (Lower limit of normal) - Signature of consent to participate in Phase II of the study Who Should NOT Join This Trial: - Known COPD - Cancer being treated - No affiliation to the social security or other social protection scheme - Pregnant or lactating woman - Patient deprived of liberty or under legal protection (under tutorship or curatorship Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: Inclusion criteria of smokers with spirometry (pre-inclusion) * Age\> 35 years * Smoking \> 20 PA * Active smoking (cessation \< 1 month) * Signature of consent to participate in Phase I of the study Inclusion criteria for patients with incidental COPD * FEV1 / FVC \<70% of the theoretical value and / or \<LLN (Lower limit of normal) * Signature of consent to participate in Phase II of the study Exclusion Criteria: * Known COPD * Cancer being treated * No affiliation to the social security or other social protection scheme * Pregnant or lactating woman * Patient deprived of liberty or under legal protection (under tutorship or curatorship

Treatments Being Tested

OTHER

Exhaustive exploration

* clinical investigations * imagery * blood assessment * functional respiratory investigations * muscle function / skeletal muscle index

Locations (1)

Hopital Henri MONDOR
Créteil, Île-de-France Region, France