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Clinical Trial Summary

The main objective of this trial is to compare the exacerbation number over 12 months of follow-up between a group of patients with COPD treated according to standardized management (azithromycin prescribed in the event of severe sputum according to the CASA-Q score , standardized comparator arm) and a similar group in which azithromycin is prescribed based on mucus rheology (experimental arm) or CASA-Q.


Clinical Trial Description

The secondary objectives are to compare between the 2 arms: - exacerbation number according to their severity (observed throughout the duration of the study); - the evolution of the symptoms, the rheology of the sputum, and the pulmonary function (measurements repeated every three months); - medication consumption and adverse events (monitored throughout the duration of the study); - patient trajectories during follow-up; - the overall clinical improvement at the end of the study and the evolution of the quality of life (measurements repeated every 3 months); - the change in biomarkers of interest (baseline versus end of study). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04339270
Study type Interventional
Source University Hospital, Montpellier
Contact Jérémy Charriot, MD
Phone 04 67 33 67 33
Email j-charriot@chu-montpellier.fr
Status Recruiting
Phase Phase 4
Start date February 3, 2023
Completion date February 2026

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