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NCT00190736 · ClinicalTrials.gov registry record · Phase 4
Efficacy and Safety of Once-Daily Atomoxetine Hydrochloride in Adults With ADHD Over an Extended Period of Time (6 Months)
A Phase 4 study, sponsored by Eli Lilly and Company.
- Completed
- Registry status
- Phase 4
- Development phase
- 440
- Enrollment target
NCT00190736: Completed Phase 4 study, sponsored by Eli Lilly and Company.
NCT00190736 is a Phase 4 study that has completed, run by Eli Lilly and Company. The registered enrollment target is 440 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (15% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00190736, a Phase 4 study, has completed, sponsored by Eli Lilly and Company.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 440 participants
- Enrollment target
Study Summary
A study to compare the effect of once-daily atomoxetine versus placebo in treating symptoms of ADHD in adults for up to 6 months.
Interventions
- DRUG placebo
- DRUG Atomoxetine Hydrochloride
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 440 participants |
| Start Date | 2004-09 |
| Est. Completion | 2006-09 |
| Phase | Phase 4 |
What the finished NCT00190736 record still lists
NCT00190736 is an interventional study that assigns participants to a tested intervention. The registered 440 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 (15% lower).
The record links to 0 conditions, and to 2 interventions - of which placebo is the first listed.
NCT00190736 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00190736 about?
NCT00190736 is a clinical study titled "Efficacy and Safety of Once-Daily Atomoxetine Hydrochloride in Adults With ADHD Over an Extended Period of Time (6 Months)". A study to compare the effect of once-daily atomoxetine versus placebo in treating symptoms of ADHD in adults for up to 6 months.
What is the current status of trial NCT00190736?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 440 participants. The study started on 2004-09. Estimated completion is 2006-09.
What interventions are being tested in trial NCT00190736?
The interventions under investigation include: placebo (DRUG), Atomoxetine Hydrochloride (DRUG).
Who is sponsoring clinical trial NCT00190736?
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 NCT00190736's enrollment target sits among peer trials
440 190th of 2000 higher than 1,810 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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