Clinical effectiveness
No statistically significant improvement was demonstrated in the primary outcome.
AZTEC asked whether giving azithromycin soon after birth could improve survival without chronic lung disease in babies born before 30 weeks’ gestation.
Adjusted OR 0.84 (95% CI 0.55–1.29), p=0.43.
The trial does not support routine early prophylactic azithromycin for all infants born before 30 weeks’ gestation as a strategy to improve the primary clinical outcome. Importantly, the trial also generated detailed safety, microbiology and antimicrobial-resistance data that continue to inform neonatal practice and future research.
No statistically significant improvement was demonstrated in the primary outcome.
The main trial did not identify a signal that changed the overall conclusion about the safety of the regimen used in AZTEC.
Laboratory analyses provide additional information on airway inflammation, Ureaplasma, microbiology and antimicrobial resistance.
A negative primary trial result can still substantially advance clinical science. AZTEC provides a large, deeply characterised neonatal cohort with linked treatment, clinical, laboratory, microbiological and follow-up data.
Studies of gut and respiratory microbiota evaluate baseline macrolide resistance and the effects of azithromycin exposure.
Follow-up at one and two years, and subsequent work, examines whether neonatal exposure is associated with later respiratory, growth, developmental or safety outcomes.
The animation summarises the trial question, intervention and principal result.
The main clinical trial was published in The Lancet Respiratory Medicine in 2024. The NIHR Health Technology Assessment report and subsequent microbiology and antimicrobial-resistance publications place the primary result in a broader evidence framework.