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A clinical trial to study the effects of nebulised hypertonic saline in bronchiolitis

Phase 4
Completed
Registration Number
CTRI/2008/091/000233
Lead Sponsor
J M Puliyel
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

All children (2 months to 2 years) admitted in pediatric ward with first episode of acute bronchiolitis

Exclusion Criteria

Children with history suggestive of chronic cardiopulmonary disease, immunodeficiency, past history of respiratory disease requiring nebulisation and critical illness

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1) Respiratory distress score<br>2) Length of hospital stayTimepoint:
Secondary Outcome Measures
NameTimeMethod
ilTimepoint: Nil
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