Last updated: October 24, 2021
Sponsor: Chinese University of Hong Kong
Overall Status: Active - Recruiting
Phase
N/A
Condition
Bronchiectasis
Treatment
N/AClinical Study ID
NCT04658277
Macrolid/Bronchiectasis/2019
Ages > 50 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Patients aged 50 years or older
- At least 2 or more exacerbation requiring antibiotic treatment in the past yearClinically stable for at least 4 weeks prior to enrollment (defined as no symptoms ofexacerbation, no requirement for supplemental antibiotic therapy)
- Diagnosis of bronchiectasis defined by high-resolution computed tomography (CT) scan
Exclusion
Exclusion Criteria:
- History of cystic fibrosis; hypogammaglobulinemia; allergic bronchopulmonaryaspergilosis,
- Cigarette smoking within 6 months
- A positive culture of non-tuberculosis mycobacteria in the past 2 years or atscreening
- Macrolide treatment for more than 3 months in the past 6 months
- Oral or intravenous courses of corticosteroids within 30 days of screening
- Any antimicrobial treatment for lower respiratory tract infection in the last 2 weeks
- Unstable arrhythmia
- History of coronary artery disease, or symptoms of heart disease
- Known allergy or intolerance to macrolides
- Patients with liver disease or with elevated transaminanse (aspartate aminotransferase (AST) and alanine aminotransferase (ALT) levels equal to or greater than the upperlimit of the normal)
- Concurrent medication: Colchicine, calcium channel blocker, statins, amiodarone,amitriptyline, trazodone, citalopram, disopyramide, itraconazole, saquinavir,ritaonavir, atazanavir, sildenafil, tadalafil, vardenafil, theophylline,carbamazepine.
Study Design
Total Participants: 40
Study Start date:
October 01, 2020
Estimated Completion Date:
September 30, 2023
Connect with a study center
Chinese University of Hong
Hong Kong, Please Select
Hong KongActive - Recruiting
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