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NCT00449527 · ClinicalTrials.gov registry record · Phase 3
A Two-week Study Assessing the Onset of Effect Questionnaire (OEQ) Administered Daily Versus Weekly in Adult Subjects
A Phase 3 study, sponsored by AstraZeneca.
- Completed
- Registry status
- Phase 3
- Development phase
- 123
- Enrollment target
NCT00449527: Completed Phase 3 study, sponsored by AstraZeneca.
NCT00449527 is a Phase 3 study that has completed, run by AstraZeneca. The registered enrollment target is 123 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (84% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00449527, a Phase 3 study, has completed, sponsored by AstraZeneca.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 123 participants
- Enrollment target
Study Summary
The purpose of this study is to demonstrate whether subjects respond similarly to the Onset of Effect Questionnaire (OEQ) using a 1 week recall period versus a 1 day recall period.
Interventions
- DRUG Budesonide HFA pMDI
- DRUG Budesonide/formoterol pMDI
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 123 participants |
| Start Date | 2007-03 |
| Est. Completion | 2007-08 |
| Phase | Phase 3 |
What the finished NCT00449527 record still lists
NCT00449527 is an interventional study that assigns participants to a tested intervention. The registered 123 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 (84% lower).
The record links to 0 conditions, and to 2 interventions - of which Budesonide HFA pMDI is the first listed.
NCT00449527 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00449527 about?
NCT00449527 is a clinical study titled "A Two-week Study Assessing the Onset of Effect Questionnaire (OEQ) Administered Daily Versus Weekly in Adult Subjects". The purpose of this study is to demonstrate whether subjects respond similarly to the Onset of Effect Questionnaire (OEQ) using a 1 week recall period versus a 1 day recall period.
What is the current status of trial NCT00449527?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 123 participants. The study started on 2007-03. Estimated completion is 2007-08.
What interventions are being tested in trial NCT00449527?
The interventions under investigation include: Budesonide HFA pMDI (DRUG), Budesonide/formoterol pMDI (DRUG).
Who is sponsoring clinical trial NCT00449527?
This trial is sponsored by AstraZeneca, which has 1,285 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00449527's enrollment target sits among peer trials
123 1615th of 2000 higher than 384 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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