Itraconazole Therapy In Bronchiectasis With Airway Mold
The primary objective of this study is to evaluate the feasibility of itraconazole therapy in patients with bronchiectasis and airway mold. Feasibility will be assessed through recruitment success, treatment adherence, tolerability, and participant retention. The study will also explore the impact on respiratory sympto
| Condition(s) | Bronchiectasis, Fungal Infection of Upper Respiratory Tract |
|---|---|
| Status | Recruiting |
| Phase | Phase 4 |
| Study type | Interventional |
| Summary | The primary objective of this study is to evaluate the feasibility of itraconazole therapy in patients with bronchiectasis and airway mold. Feasibility will be assessed through recruitment success, treatment adherence, tolerability, and participant retention. The study will also explore the impact on respiratory symptoms and airway microbiome diversity. |
| Who can participate | Inclusion Criteria: * Age ≥18 years seen at Mycobacterial and Bronchiectasis Clinic (MMBC) in Rochester * Diagnosis of bronchiectasis confirmed by MMBC provider and chest CT * Within the last 3 months - culture growth of a mold in high quantity ('many') or culture growth of at least two distinct mold species in any quantity * Not actively on antimicrobial therapy AND no current plan to initiate antimicrobial therapy at the time of enrollment, as determined by treating provider * Ability to produce spontaneous sputum at Visit 1. Exclusion Criteria: * Known diagnosis of allergic bronchopulmonary aspergillosis or invasive fungal disease * Use of the following medications: rifampin, rifabutin, phenobarbital, phenytoin, carbamazepine, dofetilide, quinidine, dronedarone, simvastatin, lovastatin, |
| Ages | 18 Years |
| Sex | All |
| Lead sponsor | Mayo Clinic |
| Locations | Rochester, Minnesota, United States |
| Start date | 2026-06-20 |
| NCT ID | NCT07283497 |
| Official listing | https://clinicaltrials.gov/study/NCT07283497 |