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Phase 2 N=40 Randomized Quadruple-blind Treatment

Azithromycin to Prevent Wheezing Following Severe Respiratory Syncytial Virus (RSV) Bronchiolitis

RSV Bronchiolitis

Enrolled (actual)
40
Serious AEs
7.7%
Results posted
Jun 2017
Primary outcome: Primary: IL-8 Concentrations — 12,795; 14,676 Pg/ml — p=0.6

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
Azithromycin (Drug); Placebo (Drug)
Age
Pediatric · 0+ yrs
Sex
All
Sponsor
Washington University School of Medicine
Primary completion
Apr 2014

Outcome Measures

OutcomeResultp-value
PRIMARY
IL-8 Concentrations
12,795; 14,676 0.6
PRIMARY
Proportion of Participants Who Experience Subsequent Recurrent (≥2) Wheezing Episodes
.50; .39
SECONDARY
Concentrations of IL-8 in Nasal Lavage on Day 15
2,318; 865
SECONDARY
Rates of Drug Related GI Side Effects.
8; 7
SECONDARY
Likelihood to Develop 3 or More Wheezing Episodes
50; 22 0.048 sig
SECONDARY
Respiratory Symptoms Following RSV Bronchiolitis
70.1; 36.7
SECONDARY
Number of Children Who Were Prescribed Inhaled Corticosteroids
6; 1
SECONDARY
Proportion of Participants With a Physician Diagnosis of Asthma
.25; .11

Summary

This trial is a proof-of-concept pilot study aim to investigate the biologic and clinical effects of early azithromycin treatment in children hospitalized with Respiratory Syncytial Virus (RSV) bronchiolitis. HYPOTHESES In infants hospitalized with RSV bronchiolitis, azithromycin therapy (compared to placebo) will result in: 1. Decreased concentrations of inflammatory mediators (IL-8 as primary outcome) in serum and nasal wash measured on day 8 after randomization. 2. A smaller proportion of participants with recurrent (≥2) wheezing episodes during weeks 3-52 following randomization.

Eligibility Criteria

Inclusion Criteria

  • Age: 1-18 months.
  • Hospitalization for the first episode of RSV bronchiolitis:
  • Confirmed RSV infection by positive nasal swab results (viral culture and/or direct antigen detection) from the SLCH virology lab; AND
  • At least two of the following symptoms/signs of bronchiolitis: respiratory rate greater than 40 breaths/minute; cough; wheezing; audible rales, crackles, and/or rhonchi; paradoxical chest movements (retractions).
  • Duration of respiratory symptoms from initiation of symptoms to admission is 5 days or less. Time of admission will define by the time the child was seen in the ED for the visit that led to hospitalization.
  • Randomization can be performed within 48 hours from time of admission (defined by time of first set of vital signs obtained on the floor).
  • Willingness to provide informed consent by the child's parent or guardian

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Exclusion Criteria

  • Prematurity (gestational age < 36 weeks).
  • Presence or history of other significant disease (CNS, lung, cardiac, renal, GI, hepatic disease, hematologic, endocrine or immune disease). Children with atopic dermatitis will not be excluded from the study.
  • Clinically significant gastroesophageal reflux currently treated with a daily anti-reflux medication (anti- H2 or PPI).
  • The child has significant developmental delay/failure to thrive, defined as weight < 3% for age and gender.
  • History of previous (before the current episode) wheeze or previous treatment with albuterol.
  • Treatment (past of present) with corticosteroid (systemic or inhaled) and/or montelukast.
  • Treatment with any antibiotics in the past 2 weeks.
  • Treatment with Macrolide antibiotic (Azithromycin, clarithromycin or erythromycin) with the past 4 weeks.
  • Current treatment with any daily medication (other then albuterol, vitamins or nutritional supplements).
  • Participation in another clinical trial.
  • Evidence that the family may be unreliable or nonadherent, or may move from the clinical center area before trial completion.
  • Contraindication of use of azithromycin or any other macrolide antibiotics.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01486758). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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