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NOT YET RECRUITING
NCT07274020
PHASE3

Long-Term Safety and Efficacy of Moxifloxacin in Bronchiectasis Patients

Sponsor: Assiut University

View on ClinicalTrials.gov

Summary

Bronchiectasis is a chronic respiratory disease characterized by recurrent infections, inflammation, and progressive lung damage. Frequent exacerbations are associated with increased morbidity, accelerated lung function decline, and reduced quality of life. Preventing exacerbations is a key therapeutic goal. Moxifloxacin, a fluoroquinolone antibiotic with broad-spectrum activity, may play a role in intermittent eradication therapy to reduce bacterial load, achieve microbiological clearance, and minimize exacerbation frequency. This randomized controlled trial will evaluate the effectiveness and safety of long-term intermittent moxifloxacin therapy compared with standard care in patients with non-cystic fibrosis bronchiectasis.

Official title: Effectiveness and Safety of Long-Term Intermittent Moxifloxacin Eradication Therapy in Non-Cystic Fibrosis Bronchiectasis: A 12-Month Randomized Controlled Trial

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

140

Start Date

2025-12-01

Completion Date

2027-01-01

Last Updated

2025-12-10

Healthy Volunteers

No

Interventions

DRUG

Intermittent Moxifloxacin + Standard Care

Moxifloxacin 400 mg orally once daily for 7 days every 8 weeks (total 6 cycles over 12 months), in addition to guideline-based standard care

OTHER

Standard Care (in control arm)

Participants will receive guideline-based management of bronchiectasis without long-term suppressive antibiotics.

Locations (1)

Assiut University hospital

Asyut, Asyut Governorate, Egypt