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Sponsor: Université de Sherbrooke
Conditions: Asthma
Interventions: Visit 1: Clinical exam and questionnaires, Visit 1: Respiratory physiology, Visit 1: Inflammometry, Visit 2: Clinical exam and questionnaires, Visit 2: Respiratory physiology
Countries: Canada
This observational study compares the phenotypic variability (clinical and biological) in treatment response to systemic corticosteroids according to the blood eosinophil count and FeNO in physician-diagnosed ≥12-year-old asthmatics presenting with an asthma attack and healthy controls. Multimodal clinical and translational assessments will be performed on 50 physician-diagnosed, ≥12-year-old asthma patients presenting with an asthma attack and 12 healthy controls. These will include a blood eosinophil count, FeNO, and testing for airway infection (conventional sputum cultures and POC nasopharyngeal swabs). People with asthma will be assessed on day 0 and after a 7-day corticosteroid course, with in-home monitoring performed in between.
Sex: ALL
Age: 12 Years to —
Healthy volunteers: Yes
Study type: OBSERVATIONAL
Inclusion Criteria: * Patients ≥12 years old with physician-diagnosed asthma for \>6 months * Experiencing an asthma attack with a patient and/or physician's decision to initiate a burst of systemic corticosteroids (but not yet started) * Assessed within 24 hours on weekdays after a screening telephone call. * For healthy volunteers: Non-atopic, non-smoking subjects with normal spirometry and no history of lung disease Exclusion Criteria: * Asthma treated with a monoclonal antibody or maintenance oral glucocorticosteroids * Current smoking * SARS-CoV-2-positive event * Significant overlapping cardiopulmonary disease (including chronic obstructive pulmonary disease, defined as age \>40 years old AND persistent airflow limitation with FEV1/FVC\<0.7 AND \>10 pack-year smoking history (or alpha-1-antitrypsin deficiency)) * Confounding immunological state * Pregnancy * Contraindication to oral corticosteroids use
- Sherbrooke, Quebec, Canada