Evaluation of Cipro Inhale in Patients With Non-cystic Fibrosis Bronchiectasis
Completed · Phase 2 · Has a placebo group
Conditions studied: Bronchiectasis
In brief
The purpose of this study is to find out if bacterial load in the airways can be reduced after inhalation of ciprofloxacin for 28 days.
Key facts
- Study ID
- NCT00930982
- Run by
- Bayer
- People needed
- 124
- Starts
- 2009-06-01
- Expected to finish
- 2010-09-01
- Last updated by the study team
- 2014-12-12
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients with a proven and documented diagnosis of non-cystic fibrosis idiopathic or post pneumonic bronchiectasis
- Stable pulmonary status and stable regimen of standard treatment at least for the past 30 days
You may not qualify if…
- Forced Expiratory Volume 1 < 35% or > 80%
- Allergic bronchopulmonary aspergillosis
- Immunodeficiency disease requiring immunoglobulin replacement
- Inflammatory bowel disease
Where it is running
- Study site — Witten, North Rhine-Westphalia, Germany
- Study site — Koblenz, Rhineland-Palatinate, Germany
- Study site — Mainz, Rhineland-Palatinate, Germany
- Study site — Geesthacht, Schleswig-Holstein, Germany
- Study site — Großhansdorf, Schleswig-Holstein, Germany
- Study site — Berlin, State of Berlin, Germany
- Study site — Berlin, State of Berlin, Germany
- Study site — Berlin, State of Berlin, Germany
- Study site — Berlin, State of Berlin, Germany
- Study site — Bad Berka, Thuringia, Germany
- Study site — Santiago de Compostela, A Coruña, Spain
- Study site — Badajoz, Badajoz, Spain
- Study site — Barcelona, Barcelona, Spain
- Study site — Palma de Mallorca, Illes Baleares, Spain
- Study site — Uppsala, Sweden
- Study site — Bristol, Avon, United Kingdom
- Study site — Cambridge, Cambridgeshire, United Kingdom
- Study site — Liverpool, Merseyside, United Kingdom
- Study site — Belfast, North Ireland, United Kingdom
- Study site — Newcastle upon Tyne, Tyne and Wear, United Kingdom
- Study site — Edinburgh, United Kingdom
- Study site — Norwich, United Kingdom
- Study site — Little Rock, Arkansas, United States
- Study site — La Jolla, California, United States
- Study site — Denver, Colorado, United States
Full record on ClinicalTrials.gov
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