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NCT00910351 · ClinicalTrials.gov registry record · Phase 1
Cipro Inhaler for Cystic Fibrosis Children Ages 6-12
A Phase 1 study, sponsored by Bayer.
- Completed
- Registry status
- Phase 1
- Development phase
- 19
- Enrollment target
NCT00910351: Completed Phase 1 study, sponsored by Bayer.
NCT00910351 is a Phase 1 study that has completed, run by Bayer. The registered enrollment target is 19 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (68% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00910351, a Phase 1 study, has completed, sponsored by Bayer.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 19 participants
- Enrollment target
Study Summary
Ciprofloxacin PulmoSphere Inhalation Powder appears to be an effective and adequate antibiotic treatment for cystic fibrosis patients with P. aeruginosa colonisation. This planned study is the first study on the use of this new Ciprofloxacin PulmoSphere Inhalation Powder in the pediatric population of 6 to 12 years of age.
Interventions
- DRUG Ciprofloxacin (Cipro, BAYQ3939)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 19 participants |
| Start Date | 2009-07 |
| Est. Completion | 2010-10 |
| Phase | Phase 1 |
What the finished NCT00910351 record still lists
NCT00910351 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 19 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (68% lower).
The record links to 0 conditions, and to 1 intervention - of which Ciprofloxacin (Cipro, BAYQ3939) is the first listed.
NCT00910351 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00910351 about?
NCT00910351 is a clinical study titled "Cipro Inhaler for Cystic Fibrosis Children Ages 6-12". Ciprofloxacin PulmoSphere Inhalation Powder appears to be an effective and adequate antibiotic treatment for cystic fibrosis patients with P. aeruginosa colonisation. This planned study is the first study on the use of this new Ciprofloxacin PulmoSphere Inhalation Powder in the pediatric population ...
What is the current status of trial NCT00910351?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 19 participants. The study started on 2009-07. Estimated completion is 2010-10.
What interventions are being tested in trial NCT00910351?
The interventions under investigation include: Ciprofloxacin (Cipro, BAYQ3939) (DRUG).
Who is sponsoring clinical trial NCT00910351?
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 NCT00910351's enrollment target sits among peer trials
19 1716th of 2000 higher than 281 of 2,000 other Phase 1 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 1 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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