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NCT00462540 · ClinicalTrials.gov registry record · Phase 3
A Crossover Study in the Treatment of Patients With COPD
A Phase 3 study, sponsored by Dey.
- Completed
- Registry status
- Phase 3
- Development phase
- 100
- Enrollment target
NCT00462540: Completed Phase 3 study, sponsored by Dey.
NCT00462540 is a Phase 3 study that has completed, run by Dey. The registered enrollment target is 100 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (87% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00462540, a Phase 3 study, has completed, sponsored by Dey.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 100 participants
- Enrollment target
Study Summary
The purpose of this study is to compare the efficacy of Formoterol Fumarate Inhalation Solution (FFIS) 20 mcg BID to Combivent® Inhalation Aerosol \[2 inhalations from metered dose inhaler (MDI)of 18 mcg ipratropium bromide and 103 mcg albuterol sulfate QID\], and to Compare the preference/compliance of BID nebulization to QID use of MDI
Interventions
- DRUG Formoterol Fumurate inhalation solution 20 mcg
- DRUG Ipratropium bromide 18 mcg and albuterol sulfate 103 mcg
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2007-05 |
| Est. Completion | 2007-10 |
| Phase | Phase 3 |
What the finished NCT00462540 record still lists
NCT00462540 is an interventional study that assigns participants to a tested intervention. The registered 100 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (87% lower).
The record links to 0 conditions, and to 2 interventions - of which Formoterol Fumurate inhalation solution 20 mcg is the first listed.
NCT00462540 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00462540 about?
NCT00462540 is a clinical study titled "A Crossover Study in the Treatment of Patients With COPD". The purpose of this study is to compare the efficacy of Formoterol Fumarate Inhalation Solution (FFIS) 20 mcg BID to Combivent® Inhalation Aerosol \[2 inhalations from metered dose inhaler (MDI)of 18 mcg ipratropium bromide and 103 mcg albuterol sulfate QID\], and to Compare the preference/complianc...
What is the current status of trial NCT00462540?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 100 participants. The study started on 2007-05. Estimated completion is 2007-10.
What interventions are being tested in trial NCT00462540?
The interventions under investigation include: Formoterol Fumurate inhalation solution 20 mcg (DRUG), Ipratropium bromide 18 mcg and albuterol sulfate 103 mcg (DRUG).
Who is sponsoring clinical trial NCT00462540?
This trial is sponsored by Dey, which has 21 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00462540's enrollment target sits among peer trials
100 1681st of 2000 higher than 288 of 2,000 other Phase 3 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 3 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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