Clinical trial
Study of Atomoxetine in Children With ADHD to Assess Symptomatic and Functional…
NCT00191633 · Eli Lilly and Company, Industry · Completed
Key facts
| NCT number | NCT00191633 |
|---|---|
| Title | Study of Atomoxetine in Children With ADHD to Assess Symptomatic and Functional Outcomes |
| Official title | A 3 Month Open-Label Study of Atomoxetine in Children With Attention-Deficit/Hyperactivity Disorder; Symptomatic and Functional Outcomes. |
| Lead sponsor | Eli Lilly and Company, Industry |
| Status | Completed |
| Phase | Phase 4 |
| Study type | Interventional |
| Conditions | Attention-Deficit/Hyperactivity Disorder |
| Intervention type | Drug |
| Interventions | Atomoxetine |
| Enrollment | 200 |
| Start date | Apr 1, 2005 |
| Completion | Jun 1, 2006 |
| First posted | Sep 19, 2005 |
| Last update posted | Jan 26, 2007 |
| Countries | Canada |
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: