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Comparing the effect of levofloxacin with azithromycin in improving pulmonary function of patients with bronchiectasis

Phase 2
Conditions
Bronchiectasis.
Bronchiectasis with (acute) exacerbation
J47.1
Registration Number
IRCT20100102002954N28
Lead Sponsor
Shahroud University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
72
Inclusion Criteria

Patients with definite diagnosis of aggravated non-fibrocystic bronchiectasis disease;
Not having moderate to severe heart failure (EF>50);
Stable vital signs;
Having a controlled and stable drug regimen (according to the opinion of a pulmonologist) during the study;
Informed consent to participate in research.

Exclusion Criteria

Gastrointestinal problems such as severe nausea and vomiting;
The presence of various cancers of the respiratory system;
The presence of chronic kidney and liver disease at the same time;
History of any surgery on the respiratory system at least in the last year;
A history of receiving any antibiotics in the last month;
A history of receiving any corticosteroid drugs in the past month;
Pregnancy and breastfeeding.

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Measuring oxygen saturation (o2sat). Timepoint: Once every two weeks. Method of measurement: Standard method with pulse oximetry device.;Measurement of lung volumes and capacities. Timepoint: Once every two weeks. Method of measurement: Standard method with spirometer.
Secondary Outcome Measures
NameTimeMethod
Measuring discomfort from breathing (Dyspnea). Timepoint: Once every two weeks. Method of measurement: Using standard Borg questionnaire.;Measurement of white blood cells. Timepoint: Once every two weeks. Method of measurement: By standard laboratory method.
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