Influenza Clinical Trial
Official title:
Anti-inflammatory Effects of Macrolide Treatment in Influenza Lower Respiratory Tract Infections
Influenza lower respiratory tract infection (LRTI) is a major cause of morbidity and mortality worldwide. While viral replication can be suppressed by antiviral treatment, excessive inflammatory responses, which are increasingly recognized to contribute to severe influenza complications, remain unopposed. Macrolides have been used widely to treat community-acquired pneumonia, and shown to exert anti-inflammatory effects in other respiratory diseases, providing clinical benefits. In this randomized, open-label, multicenter study, we aim to investigate the anti-inflammatory effects of macrolide treatment in influenza LRTI. Its impacts on the cytokine response, viral clearance, symptoms and disease resolution will be studied. Such results may lead to the development of new therapeutic approaches against severe influenza infection, and provide better insights into disease pathogenesis.
Objectives: (1) We aim to investigate the anti-inflammatory effects of macrolide treatment
in patients with influenza LRTI and the impact on viral clearance. (2) To investigate the
impact of macrolide treatment on influenza symptom and disease resolution.
Design: A randomized, open-label, multicenter study.
Settings: Acute medical facilities in 3 general public hospitals in Hong Kong.
Subjects, Sampling and Intervention: Adult (>/=18 years) patients hospitalized for
virologically confirmed influenza LRTI who fulfill the inclusion/exclusion criteria will be
randomized to receive (1) azithromycin 500 mg p.o. for 5 days (in addition to antiviral, as
part of usual care), or (2) no azithromycin (ie, antiviral alone, part of usual care) after
informed consent. Serial blood samples will be collected for cytokine/inflammatory response
assays. Serial nasopharyngeal swabs will be collected to assess for viral clearance.
Symptoms, clinical progress, radiography and adverse events will be monitored.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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