The effect of 3% hypertonic saline and salbutamol in treatment of patients with acute bronchiolitis
Not Applicable
- Conditions
- Acute bronchiolitis.Acute bronchiolitis
- Registration Number
- IRCT2015092214333N39
- Lead Sponsor
- Vice chancellor for research, Kermanshah University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 64
Inclusion Criteria
children under 2 years old; children with acute bronchiolitis.
Exclusion criteria: children with cystic fibrosis; bronchopulmonary dysplasia and those with heart disease; premature babies with GA=34; patients who had used steroids during the last 48 hours prior to admission; children with immunodeficiency.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Chest auscultation in terms of wheezing. Timepoint: Beginning and end of study. Method of measurement: By a doctor.;Cough. Timepoint: Beginning and end of study. Method of measurement: By doctor and counting.;Respiratory rate. Timepoint: Beginning and end of study. Method of measurement: By doctor and counting.;Blood oxygen saturation. Timepoint: Beginning and end of study. Method of measurement: By pulse oximeter.;Lung retraction. Timepoint: Beginning and end of study. Method of measurement: Based on physician observation.;The temperature of patient. Timepoint: Beginning and end of study. Method of measurement: Thermometer device.;Overall health of Patient. Timepoint: Beginning and end of study. Method of measurement: Based on physician observation and patient interview.;The severity of bronchiolitis. Timepoint: Beginning and end of study. Method of measurement: Based on the observations and examined by a doctor.
- Secondary Outcome Measures
Name Time Method