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Use of Clarithromycin in Mustard-Induced Bronchiolitis

Phase III, Randomized, Double Blind Study of Low Dose Long Term Clarithromycin Versus Placebo in Treatment of Chronic Pulmonary Lesions Due to Sulfur Mustard

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00381147
Enrollment
Unknown
Registered
2006-09-27
Start date
Unknown
Completion date
Unknown
Last updated
2009-01-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Obliterating Bronchiolitis, Bronchiolitis Obliterans

Brief summary

We looked for the effectiveness of low-dose long-term prescription of clarithromycin in mustard-induced chronic pulmonary lesions, especially bronchiolitis obliterans

Interventions

DRUGClarithromycin

Sponsors

Baqiyatallah Medical Sciences University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE

Eligibility

Sex/Gender
MALE

Inclusion criteria

* His/her own will to participate * Documented chemical exposure * Clinical, spirometric and radiological findings were compatible with BO on High Resolution Computed Tomography (HRCT)

Exclusion criteria

* any drug reactions during the trial * history of sensitivity to macrolides * diarrhea, gray stool, jaundice, eosinophilia, acute cholestatic hepatitis, pruritis, dark urine, abdominal pain, osteomatosis, depression, taste change, behavioural changes, early fatigue, odynophagia, glossitis , dizziness * co-adminstration of: terfenadine, theophylline, carbamazepine, ergotamine, dihydroergotamine, warfarin, cisapride, digoxin, triazolam, phenytoin, steroids, any immunosuppressive, any systemic antibiotics * using drugs that he/she cannot discontinue * using drugs with potential interaction * subject will to exit from the trial * history of lobe resection of lung * history of exacerbation in the last month prior to the beginning of trial * continuous need to oxygen * use of corticosteroids in last week prior to the trial beginning * Radiographic evidence of pneumonia, active tuberculosis, lung carcinoma, or an infection that necessitated the use of an antibiotic * exacerbating of subjects * creatinine srum level more than normal * increasing ALT, AST levels * total bilirubin more twice than normal * subjects who did not use their drugs properly

Countries

Iran

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026