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NCT00486122 · ClinicalTrials.gov registry record · Phase 4
Evaluation of Continuous Symptom Treatment of ADHD
A Phase 4 study, sponsored by Eli Lilly and Company.
- Completed
- Registry status
- Phase 4
- Development phase
- 282
- Enrollment target
NCT00486122: Completed Phase 4 study, sponsored by Eli Lilly and Company.
NCT00486122 is a Phase 4 study that has completed, run by Eli Lilly and Company. The registered enrollment target is 282 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (46% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00486122, a Phase 4 study, has completed, sponsored by Eli Lilly and Company.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 282 participants
- Enrollment target
Study Summary
The purpose of this study is to test the hypothesis that atomoxetine administered orally, once a day, at doses up to 1.4 mg/kg/day for approximately 6 weeks given in the morning is superior to placebo in children with ADHD.
Interventions
- DRUG Placebo
- DRUG Atomoxetine Hydrochloride
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 282 participants |
| Start Date | 2003-09 |
| Est. Completion | 2004-06 |
| Phase | Phase 4 |
What the finished NCT00486122 record still lists
NCT00486122 is an interventional study that assigns participants to a tested intervention. The registered 282 participants enrollment target is mid-sized for trials with a published cap, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (46% lower).
The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.
NCT00486122 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00486122 about?
NCT00486122 is a clinical study titled "Evaluation of Continuous Symptom Treatment of ADHD". The purpose of this study is to test the hypothesis that atomoxetine administered orally, once a day, at doses up to 1.4 mg/kg/day for approximately 6 weeks given in the morning is superior to placebo in children with ADHD.
What is the current status of trial NCT00486122?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 282 participants. The study started on 2003-09. Estimated completion is 2004-06.
What interventions are being tested in trial NCT00486122?
The interventions under investigation include: Placebo (DRUG), Atomoxetine Hydrochloride (DRUG).
Who is sponsoring clinical trial NCT00486122?
This trial is sponsored by Eli Lilly and Company, which has 1,341 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00486122's enrollment target sits among peer trials
282 303rd of 2000 higher than 1,698 of 2,000 other Phase 4 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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