Children with lung and airway malformations or early structural lung damage face significant challenges, often leading to recurrent respiratory infections, hospitalizations, and decreased quality of life. Despite various interventions, effective strategies are urgently needed.
The link between these conditions and persistent bacterial bronchitis remains unclear, possibly due to compromised airways and reduced mucociliary clearance. Although antibiotics can alleviate symptoms, relapse is common.
Experts often prescribe prophylactic azithromycin, despite limited evidence of its benefits. Azithromycin shows promise due to its anti-inflammatory and immunomodulatory effects but lacks thorough evaluation in this population.
To address this gap, we propose a double-blind, randomized controlled trial to assess azithromycin's effectiveness and safety in preventing respiratory infections in children with these conditions. This research aims to inform clinical practice and improve the health of affected children and their families.
CT and bronchoscopy verified and structural lung damage or congenital lung and airway malformations
Outpatient affiliation with one of the three highly specialized pediatric pulmonology centers.
At risk of or already documented respiratory infections requiring antibiotics.
Age between 0-72 months at inclusion.
Asthmatic challenges: Patients without any of the conditions mentioned in table 1 repeatedly experiencing asthmatic problems are not eligible for this study.
Cystic fibrosis (CF) or primary ciliary dyskinesia (PCD): Patients with a CF or PCD diagnosis will be excluded.
Impaired liver function: Children with an alanine transaminase (ALAT) twice or more the upper limits of normal will be excluded.
Impaired kidney function: Children with a serum creatinine higher than the upper limit of normal for age will be excluded.
Parallel
Azithromycin 40 MG/ML
DrugMaintenance Antibiotic treatment
Placebo
Other interventionPlacebo
Incidence of exacerbations
Number of exacerbations where systemic antibiotics is needed within the study period
Severity of exacerbations
Duration of exacerbations, hospitalizations and durations of hospitalizations
Lung function measures
Impulse oscillometry (IOS) measurement pre- and post drug administrations
Quality of Life
Questionaire on a Likert scale 0-5. Using PedsQL(TM).
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This trial is not recruiting at the moment. You can still explore other options:
