Clinical trial
Evaluation of Continuous Symptom Treatment of ADHD
NCT00486122 · Eli Lilly and Company, Industry · Completed
Key facts
| NCT number | NCT00486122 |
|---|---|
| Title | Evaluation of Continuous Symptom Treatment of ADHD |
| Official title | Evaluation of Continuous Symptom Treatment of ADHD: A Placebo-Controlled Double-Blind Assessment of Morning-Dosed or Evening-Dosed Strattera |
| 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, Placebo |
| Enrollment | 282 |
| Start date | Sep 1, 2003 |
| Completion | Jun 1, 2004 |
| 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: