Evaluation of HFCWO using The Vest System for Treatment of Non-Cystic Fibrosis Bronchiectasis in the home setting
Are you eligible to participate in this study?
You may be eligible for this study if you meet the following criteria:
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Conditions: Bronchiectasis
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Age: Between 18 - 80 Years
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Gender: Male or Female
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Other Inclusion Criteria:
- Subjects with radiological diagnosis of NCFBE based on high resolution chest CT scan
- Subjects with history of at least 2 acute exacerbations or hospitalization in the past 12 months
- Subjects who are clinically stable for more than 2 weeks
- Subjects are able to provide signed informed consent
You may not be eligible for this study if the following are true:
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• Diagnosis of Cystic Fibrosis • History of bronchiectasis secondary to primary immunodeficiency
- Subjects with active pulmonary tuberculosis
- Subjects on active treatment of Non-Tuberculous Mycobacterium (NTM)
- Subjects who are currently on HFCWO treatment
- Subjects who are diagnosed comorbidity or medical indication that would prevent study completion
- Subjects with history of pneumothorax within past 6 months
- Subjects with history of hemoptysis requiring embolization within past 12 months
- Subjects inability to perform HFCWO therapy or OPEP therapy as directed
- Pregnancy or lactation
- Subjects with inability or unwillingness to complete study visits or provide follow-up data as required by the study protocol
If you are registered as a volunteer, please log in to contact the study team/express interest in this study.