Clinical trial
Efficacy and Safety of Once-Daily Atomoxetine Hydrochloride in Adults With ADHD…
NCT00190736 · Eli Lilly and Company, Industry · Completed
Key facts
| NCT number | NCT00190736 |
|---|---|
| Title | Efficacy and Safety of Once-Daily Atomoxetine Hydrochloride in Adults With ADHD Over an Extended Period of Time (6 Months) |
| Official title | Efficacy and Safety of Once-Daily Atomoxetine Hydrochloride in Adults With ADHD Over an Extended Period of Time (6 Months); With a Brief Evaluation of Executive Cognition |
| Lead sponsor | Eli Lilly and Company, Industry |
| Status | Completed |
| Phase | Phase 4 |
| Study type | Interventional |
| Conditions | ADHD |
| Intervention type | Drug |
| Interventions | Atomoxetine Hydrochloride, placebo |
| Enrollment | 440 |
| Start date | Sep 1, 2004 |
| Completion | Sep 1, 2006 |
| First posted | Sep 19, 2005 |
| Last update posted | Nov 6, 2007 |
| 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: