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…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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