Clinical trial
Safety and Efficacy of Switching From a Stimulant Medication to Atomoxetine in…
NCT00485875 · Eli Lilly and Company, Industry · Completed
Key facts
| NCT number | NCT00485875 |
|---|---|
| Title | Safety and Efficacy of Switching From a Stimulant Medication to Atomoxetine in Children and Adolescents With ADHD |
| Official title | An Open-Label, Multicenter, Pilot Study of the Safety and Efficacy of Transitioning From a Stimulant Medication to Atomoxetine in Pediatric and Adolescent Outpatients With DSM-IV Attention-Deficit/Hyperactivity Disorder (ADHD) |
| 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 Hydrochloride |
| Enrollment | 62 |
| Start date | Jun 1, 2004 |
| Completion | Jan 1, 2005 |
| First posted | Jun 13, 2007 |
| Last update posted | Jun 13, 2007 |
| Countries | United States |
At a glance
- 1–9 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: