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Clinical Trial Summary

Our long-term goal is to more precisely define the role of mass azithromycin treatments as an intervention for reducing childhood mortality. We propose a single multi-site (multi-country), cluster-randomized trial comparing communities randomized to oral azithromycin with those randomized to placebo. We hypothesize that mass azithromycin treatments will reduce childhood mortality.


Clinical Trial Description

We will assess childhood mortality over three years, comparing communities where children aged 1-60 months receive biannual oral azithromycin ("Azithromycin" arm) for two years, to communities where the children receive biannual oral placebo ("Control" arm) for two years. During the third year at the Niger site only, everyone will receive azithromycin. This is a cluster-randomized trial; at each site, communities within a contiguous area of 300,000 to 600,000 individuals will be randomized to azithromycin or placebo using simple random sampling. Niger contingency study: In the event that mass distributions of oral azithromycin are proven to reduce mortality in 1-60 month-old children, then we will treat all communities in Niger with mass azithromycin distributions to test whether the intervention continues to reduce childhood mortality after the initial 2 years of mass treatments. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02047981
Study type Interventional
Source University of California, San Francisco
Contact
Status Completed
Phase Phase 4
Start date December 2014
Completion date September 2018

See also
  Status Clinical Trial Phase
Completed NCT03338244 - Mortality Reduction After Oral Azithromycin Contingency: Mortality Study Phase 4
Completed NCT02048007 - Mortality Reduction After Oral Azithromycin: Morbidity Study Phase 4
Completed NCT03676764 - Community Health Azithromycin Trial in Burkina Faso Phase 4
Completed NCT03682653 - Neonates and Azithromycin, an Innovation in the Treatment of Children in Burkina Faso Phase 4