Anti-inflammatory Effects of Macrolide Treatment in Influenza Lower Respiratory Tract Infections

Sponsor
Chinese University of Hong Kong (Other)
Overall Status
Completed
CT.gov ID
NCT01779570
Collaborator
(none)
68
2
2
37.9
34
0.9

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Drug: Macrolide treatment
Phase 4

Detailed Description

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.

Study Design

Study Type:
Interventional
Actual Enrollment :
68 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Anti-inflammatory Effects of Macrolide Treatment in Influenza Lower Respiratory Tract Infections
Study Start Date :
Feb 1, 2013
Actual Primary Completion Date :
Apr 1, 2016
Actual Study Completion Date :
Apr 1, 2016

Arms and Interventions

Arm Intervention/Treatment
Experimental: Macrolide treatment

Azithromycin 500 mg daily for 5 days

Drug: Macrolide treatment

No Intervention: No macrolide treatment

No azithromycin

Outcome Measures

Primary Outcome Measures

  1. cytokine and inflammatory responses [within 10 days post-intervention]

    Serial measurements of selected cytokines/chemokines (e.g. interleukin-6, CXCL8) and proinflammatory molecules (e.g. DAMPs)

Secondary Outcome Measures

  1. viral clearance [within 10 days post-intervention]

    Viral RNA and culture negativity in serially collected respiratory tract specimens

Other Outcome Measures

  1. time to recovery [within 10 days post-intervention]

    e.g. time to symptom resolution, time to hospital discharge, etc

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. established influenza A or B infection by virologic tests

  2. age >/=18 years

  3. present within 4 days from illness onset

  4. clinical evidence of LRTI and require hospital care

  5. require antiviral (oseltamivir) treatment

  6. able to provide written, informed consent.

Exclusion Criteria:
  1. patients on immunosuppressants

  2. pregnant or lactating woman

  3. known hepatic failure, end-stage renal failure, cardiac arrhythmia (e.g. prolonged corrected QT interval >450 msec)

  4. known contraindications to azithromycin (e.g. allergic reaction)

  5. lack of consent for study.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Prince of Wales Hospital Hong Kong Hong Kong
2 Princess Margaret Hospital Hong Kong Hong Kong

Sponsors and Collaborators

  • Chinese University of Hong Kong

Investigators

  • Principal Investigator: Nelson LS Lee, MD, Chinese University of Hong Kong

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

Responsible Party:
Nelson Lee, Professor, Chinese University of Hong Kong
ClinicalTrials.gov Identifier:
NCT01779570
Other Study ID Numbers:
  • RGC CUHK468112
First Posted:
Jan 30, 2013
Last Update Posted:
Jul 27, 2016
Last Verified:
Jul 1, 2016
Keywords provided by Nelson Lee, Professor, Chinese University of Hong Kong
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 27, 2016