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NCT00930982 · ClinicalTrials.gov registry record · Phase 2
Evaluation of Cipro Inhale in Patients With Non-cystic Fibrosis Bronchiectasis
A Phase 2 study, sponsored by Bayer.
- Completed
- Registry status
- Phase 2
- Development phase
- 124
- Enrollment target
NCT00930982: Completed Phase 2 study, sponsored by Bayer.
NCT00930982 is a Phase 2 study that has completed, run by Bayer. The registered enrollment target is 124 participants, roughly in line with the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00930982, a Phase 2 study, has completed, sponsored by Bayer.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 124 participants
- Enrollment target
Study Summary
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.
Primary Outcome
Total bacterial load was determined in sputum collected before the inhalation of study drug. Sputum samples were either provided by the participant during the respective study visit, or participants had to bring a sputum sample that had been produced within the 4 hours prior to the visit. Induced sputum samples could be collected if the participant was unable to produce a spontaneously expectorated sputum sample of \> 2 mL. Imputation method: last observation carried forward (LOCF). CFU: colony
Interventions
- DRUG Placebo
- DRUG Ciprofloxacin (Cipro, BAYQ3939)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 124 participants |
| Start Date | 2009-06 |
| Est. Completion | 2010-09 |
| Phase | Phase 2 |
What the finished NCT00930982 record still lists
NCT00930982 is an interventional study that assigns participants to a tested intervention. The registered 124 participants enrollment target is mid-sized for trials with a published cap, roughly in line with the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target.
The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.
NCT00930982 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00930982 about?
NCT00930982 is a clinical study titled "Evaluation of Cipro Inhale in Patients With Non-cystic Fibrosis Bronchiectasis". 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.
What is the current status of trial NCT00930982?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 124 participants. The study started on 2009-06. Estimated completion is 2010-09.
What interventions are being tested in trial NCT00930982?
The interventions under investigation include: Placebo (DRUG), Ciprofloxacin (Cipro, BAYQ3939) (DRUG).
Who is sponsoring clinical trial NCT00930982?
This trial is sponsored by Bayer, which has 591 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00930982's enrollment target sits among peer trials
124 564th of 2000 higher than 1,437 of 2,000 other Phase 2 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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