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Evaluation of the effect of oral monte locust in the treatment of acute asthma in childre

Phase 3
Conditions
Asthma.
Asthma
Registration Number
IRCT20200412047048N1
Lead Sponsor
Tehran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
100
Inclusion Criteria

All patients aged 1-14 years who are confirmed based on history and examination for asthma attack

Exclusion Criteria

Those with a history of taking corticosteroids or montelukast for the past ten days
All patients who developed a diagnosis other than asthma, such as pneumonia or bronchiolitis

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Asthma. Timepoint: At the beginning of the patient's visit, 1,4,8,24,48 hours after the intervention and one week after discharge from the hospital. Method of measurement: Patient scoreboard.
Secondary Outcome Measures
NameTimeMethod
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