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Recruiting
NCT04339270
Chronic Airway Disease, Mucus Rheology and Exacerbations
Conditions: Chronic Obstructive Pulmonary Disease
Sex: All
Ages: 40 Years – 85 Years
Healthy volunteers: No
Phase: PHASE4
Enrollment: 72
Sponsor: University Hospital, Montpellier
Location: University Hospitals of Bordeaux Bordeaux
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.
Eligibility Criteria
Inclusion Criteria:
* Subjets between 40 - 85 years (included)
* Written and signed informed consent form
* Subjects must be able to attend all planned visits and comply with all test procedures
* Beneficiary of or affiliated with the French social security system
* Man or woman with chronic obstructive pulmonary disease for at least 1 year defined according to Global Initiative for Chronic Obstructive Lung Disease (GOLD) criteria and validated by the clinical investigator
* Optimal treatment according to GOLD class severity C or D recommendations
* \>=3 exacerbation (regardless of severity: mild-moderate-severe) or ≥ 1 severe exacerbations (requiring hospitalization) in the past 12 months
* Spontaneous or induced sputum production
* Electrocardiogram: corrected distance between Q and T waves (QTC) \
Source: ClinicalTrials.gov (NCT04339270). StuddyBuddy aggregates publicly available trial information.