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The azithromycin to prevent wheezing following severe RSV bronchiolitis-II clinical trial: Rationale, study design, methods, and characteristics of study population
- Source :
- Contemporary Clinical Trials Communications, Contemporary Clinical Trials Communications, Vol 22, Iss, Pp 100798-(2021)
- Publication Year :
- 2020
-
Abstract
- Severe respiratory syncytial virus (RSV) bronchiolitis in early life is a significant risk factor for future recurrent wheeze (RW) and asthma. The goal of the Azithromycin to Prevent Wheezing following severe RSV bronchiolitis II (APW-RSV II) clinical trial is to evaluate if azithromycin treatment in infants hospitalized with RSV bronchiolitis reduces the occurrence of RW during the preschool years. The APW-RSV II clinical trial is a double-blind, placebo-controlled, parallel-group, randomized trial, including otherwise healthy participants, ages 30 days-18 months, who are hospitalized due to RSV bronchiolitis. The study includes an active randomized treatment phase with azithromycin or placebo for 2 weeks, and an observational phase of 18–48 months. Two hundred participants were enrolled during three consecutive RSV seasons beginning in the fall of 2016 and were randomized to receive oral azithromycin 10 mg/kg/day for 7 days followed by 5 mg/kg/day for an additional 7 days, or matched placebo. The study hypothesis is that in infants hospitalized with RSV bronchiolitis, the addition of azithromycin therapy to routine bronchiolitis care would reduce the likelihood of developing post-RSV recurrent wheeze (≥3 episodes). The primary clinical outcome is the occurrence of a third episode of wheezing, which is evaluated every other month by phone questionnaires and during yearly in-person visits. A secondary objective of the APW-RSV II clinical trial is to examine how azithromycin therapy changes the upper airway microbiome composition, and to determine if these changes are related to the occurrence of post-RSV RW. Microbiome composition is characterized in nasal wash samples obtained before and after the study treatments. This clinical trial may identify the first effective intervention applied during severe RSV bronchiolitis to reduce the risk of post-RSV RW and ultimately asthma.
- Subjects :
- AESI, AEs of Special Interest
Medicine (General)
Pediatrics
AE, Adverse events
Azithromycin
law.invention
0302 clinical medicine
RBEL, RSV Bronchiolitis in Early Life
Randomized controlled trial
law
ED, Emergency department
Medicine
IL, Interleukin
030212 general & internal medicine
DSMB, Data safety and monitoring board
General Medicine
respiratory system
Respiratory syncytial virus (RSV) bronchiolitis
SAE, serious adverse events
Population study
RSV, Respiratory syncytial virus
medicine.drug
NHLBI, National Heart, Lung, and Blood Institute
RZ, Randomization
medicine.medical_specialty
PC, Phone call
IRB, Institutional review board
Placebo
Article
ICS, Inhaled corticosteroids
03 medical and health sciences
R5-920
MMP-9, Matrix metallopeptidase-9
APW, Azithromycin to Prevent Wheezing
Asthma
Pharmacology
RW, Recurrent wheezing
business.industry
LRTI, Lower respiratory tract infection
medicine.disease
AZM, Azithromycin
SLCH, Saint Louis Children's Hospital
Clinical trial
Recurrent wheezing
Bronchiolitis
Observational study
V, visit
Microbiome
business
030217 neurology & neurosurgery
Subjects
Details
- ISSN :
- 24518654
- Volume :
- 22
- Database :
- OpenAIRE
- Journal :
- Contemporary clinical trials communications
- Accession number :
- edsair.doi.dedup.....e349b52cc7826c454006f4e6035f412a