Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE4
INTERVENTIONAL
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
SINGLE_GROUP
TREATMENT
DOUBLE
Interventions
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Erythromycin
Eligibility Criteria
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Inclusion Criteria
* Clinical, spirometric and radiological findings were compatible with BO on High Resolution Computed Tomography (HRCT)
* Non-responsiveness to high dose bronchodilator therapy
Exclusion Criteria
* History of cigarette smoking and occupational exposure to toxic agents of hypersensitivity to macrolides
* History of treatment with a systemic antibiotic within 7 days before the start of the study
* Any investigational medicine within 4 weeks of the study
* History of antibiotic injection within 6 weeks before the study
* Concomitant Theophylline or Carbamazepine, unless their serum concentrations were regularly monitored
* Patients who were in the exacerbation phase of their respiratory complications
* Need to use medications interact with macrolides such as Digoxin, Theophylline and Carbamazepine
* Systemic antibiotics
* Systemic Corticosteroids
* Admission to the hospital
* Abnormal kidney or liver function
MALE
No
Sponsors
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Baqiyatallah Medical Sciences University
OTHER
Principal Investigators
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Mostafa Ghanei, Professor
Role: STUDY_DIRECTOR
Research Center of Chemical Injuries, Baqyatallah Medical Sciences University, Tehran, Iran
Locations
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Baqiyatallah Medical Sciences University
Tehran, Tehran Province, Iran
Countries
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Other Identifiers
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S-340-14-6-1-PU-02
Identifier Type: -
Identifier Source: org_study_id