Clinical trial
A Two-week Study Assessing the Onset of Effect Questionnaire Administered…
NCT00449501 · AstraZeneca, Industry · Completed
Key facts
| NCT number | NCT00449501 |
|---|---|
| Title | A Two-week Study Assessing the Onset of Effect Questionnaire Administered Pre-dose Versus Post-dose in Adult Subjects |
| Official title | A Two-week, Randomised, Double-blind Study Assessing the Onset of Effect Questionnaire Administered Pre-dose Versus Post-dose in Adult Subjects (≥ 18 Years) With Mild to Moderate Asthma, Receiving SYMBICORT® pMDI 80/4.5 μg x 2 Actuations Twice Daily or Budesonide HFA pMDI 80 μg x 2 Act. Twice Daily |
| Lead sponsor | AstraZeneca, Industry |
| Status | Completed |
| Phase | Phase 3 |
| Study type | Interventional |
| Conditions | Asthma |
| Intervention type | Drug |
| Interventions | Budesonide/formoterol pMDI, Budesonide HFA pMDI |
| Enrollment | 134 |
| Start date | Mar 1, 2007 |
| Completion | Nov 1, 2007 |
| First posted | Mar 20, 2007 |
| Last update posted | Jan 24, 2011 |
| Countries | United States |
At a glance
- 10–99 Study sites
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: