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Evaluation of the effect of budesonide nebulizer in patients with exacerbated COPD

Phase 2
Recruiting
Conditions
Chronic obstructive pulmonary disease.
Chronic obstructive pulmonary disease with (acute) exacerbation
Registration Number
IRCT20180523039800N1
Lead Sponsor
Tehran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
80
Inclusion Criteria

Patients with exacerbated COPD following respiratory infection
15-70 years old
Disease severity of moderate to severe based on GOLD scoring

Exclusion Criteria

Exacerbated COPD with a cause other than respiratory infection
History of asthma, allergic rhinitis or atopy
History of systemic corticosteroids more than 1500 micrograms/ day over the past month
Patients with decreased consciousness
Known psychological disorder and inability to cooperate in the study

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Variation in peak expiratory flow rate. Timepoint: 30 and 60 minutes, and 3, 6, 12, and 24 hours later. Method of measurement: Peak flow meter device.
Secondary Outcome Measures
NameTimeMethod
Variation in FEV1 percentage. Timepoint: 30 and 60 minutes and 3, 6, 12 and 24 hours later. Method of measurement: Spirometry.
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