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Comparision of low dose (200 mcg) versus high dose (400mcg) bronchodilator response in asthmatic childre

Not Applicable
Conditions
Health Condition 1: J459- Other and unspecified asthma
Registration Number
CTRI/2024/04/065106
Lead Sponsor
Department of Pediatrics
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

FEV1/FVC ratio lower than 90%

Exclusion Criteria

bronchodilators taken before PFT

Children with underlying chronic disease

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To compare improvement in FEV1 from baseline after inhalation of different doses <br/ ><br>(400mcg and 200 mcg) of salbutamolTimepoint: 12 months
Secondary Outcome Measures
NameTimeMethod
Proportions of children having more than 12% BDR in both the groups <br/ ><br>To assess improvement in PEF, FEF 25 to 75 in both groups <br/ ><br>To assess adverse effects in both groupsTimepoint: 12 months
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