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Azithromycin Treatment for Respiratory Syncytial Virus-induced Respiratory Failure in Children
Sponsor: University of Alabama at Birmingham
Summary
The overarching hypothesis of the ARRC trial is that administration of Azithromycin (AZM) during acute, Respiratory Syncytial Virus (RSV)-induced respiratory failure will be beneficial, mediated through the matrix metalloproteinase (MMP)-9 pathway.
Key Details
Gender
All
Age Range
3 Days - 2 Years
Study Type
INTERVENTIONAL
Enrollment
370
Start Date
2022-02-27
Completion Date
2028-07-31
Last Updated
2026-02-09
Healthy Volunteers
No
Conditions
Interventions
AZM Group
AZM at 20 mg/kg will be given intravenous daily for 3 days once patients are consented and enrolled into the study.
Control Group
Saline will be given intravenous daily for 3 days once patients are consented and enrolled into the study.
Locations (15)
The University of Alabama at Birmingham
Birmingham, Alabama, United States
University of California San Francisco
San Francisco, California, United States
Yale School of Medicine
New Haven, Connecticut, United States
Children's National Hospital
Washington D.C., District of Columbia, United States
Ann & Robert H. Lurie Children's Hospital of Chicago
Chicago, Illinois, United States
Riley Children's Health
Indianapolis, Indiana, United States
St. Louis Children's Hospital
St Louis, Missouri, United States
University of Nebraska Medical Center
Omaha, Nebraska, United States
University of North Carolina at Chapel Hill
Chapel Hill, North Carolina, United States
Rainbow Babies and Children's Hospital
Cleveland, Ohio, United States
Nationwide Children's Hospital
Columbus, Ohio, United States
Oklahoma Health Sciences
Oklahoma City, Oklahoma, United States
Children's Hospital of Philadelphia
Philadelphia, Pennsylvania, United States
The University of Texas Southwestern Medical Center
Dallas, Texas, United States
University of Utah
Salt Lake City, Utah, United States