About this trial
The goal of this clinical trial is to compare the efficacy of hypertonic saline nebulization with adrenaline nebulization in the treatment of acute bronchiolitis in children. Main aim is to evaluate the following in both group of patients
1. Improvement in Wood-Downes clinical score (WDF score) in bronchiolitis 2. Length of Hospitalization
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
All children admitted in PICU with acute bronchiolitis
Disqualifiers
children with co-exiting illnesses like
Congenital Heart Disease
Immunodeficiency
other Infectious disease like Meningitis, encephalitis, Pneumonia, TORCH
Trial design
Parallel
Treatments tested in this trial
Hypertonic Saline Solution, 1 Ml
DrugDilute 0.3 ml hypertonic saline with 3 ml normal saline for nebulization
Adrenaline
Drugdilute 0.3 ml adrenaline with 3 ml normal saline for nebulization
Treatment groups
Trial outcomes
Primary outcomes
Wood-Downes-Ferres clinical score calculation
A score of 0-3 mild, 4-6 moderately ill, \>6 severely ill
Secondary outcomes
total length of hospitalization
less than 1 week, more than 1 week,
Sponsors and contacts
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