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Comparing Therapeutic effects of combination of high volume normal saline and salbutamol nebulizer with combination of hypertonic saline 3% and salbutamol nebulizer in bronchiolitis treatment

Phase 3
Conditions
Bronchiolitis.
Other acute lower respiratory infections
J20, J21,J
Registration Number
IRCT2016022826809N1
Lead Sponsor
Vice chancellor for research,Zahedan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
180
Inclusion Criteria

age less than 2 year old; history of recent upper respiratory viral infection which caused wheeze and crackle in auscultation; CBSS 4-8 in admit. Exclusion criteria: age less than 1 month or more than 2 years old; history of recurrent attack of wheeze; sever neurological disorder; consolidation in Chest x ray; immune deficiency; congenital heart disease; history of premature (gestational age less than 34 weeks); birth weight less than 2500 gr; saturation of oxygen less than 85% in room; CBSS less than 4 or more than 8; unstable hemodynamic (heart rate more than 200 per minute, blood pressure 2 standard deviation more or less than normal range for age and sex, respiratory rate more than 70 per minute).

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Respiratory rate. Timepoint: Pretreatment and each 30 minute up to 3 times after the begining of treatment. Method of measurement: Counting respiratory rate in 1 minute.;O2 saturation. Timepoint: Pretreatment and each 30 minute up to 3 times after the begining of treatment. Method of measurement: Pulse oximetery.;Heart rate. Timepoint: Pretreatment and each 30 minute up to 3 times after the begining of treatment. Method of measurement: Counting heart rate in 1 minute.;Intercostal retraction. Timepoint: Pretreatment and each 30 minute up to 3 times after the begining of treatment. Method of measurement: Physical exam and score of CBSS (0,1,2,3).;Dyspnea. Timepoint: Pretreatment and each 30 minute up to 3 times after the begining of treatment. Method of measurement: Physical exam and score of CBSS (0,1,2,3).;Wheezing. Timepoint: Pretreatment and each 30 minute up to 3 times after the begining of treatment. Method of measurement: Physical exam and score of CBSS (0,1,2,3).
Secondary Outcome Measures
NameTimeMethod
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