Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT00418262 · ClinicalTrials.gov registry record · Phase 3
Open-Label Study of the Long Term Tolerability and Safety of Atomoxetine in Children With FASD and ADD/ADHD
A Phase 3 study, sponsored by University of Oklahoma.
- Completed
- Registry status
- Phase 3
- Development phase
- 27
- Enrollment target
NCT00418262: Completed Phase 3 study, sponsored by University of Oklahoma.
NCT00418262 is a Phase 3 study that has completed, run by University of Oklahoma. The registered enrollment target is 27 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00418262, a Phase 3 study, has completed, sponsored by University of Oklahoma.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 27 participants
- Enrollment target
Study Summary
Determine if atomoxetine is safe and well tolerated by children with fetal alcohol syndrome.
Primary Outcome
Motor Tics Parent rating of none (0), mild (1) , moderate (2) or severe (3) for each manifestation
Interventions
- DRUG Atomoxetine
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 27 participants |
| Start Date | 2005-08 |
| Est. Completion | 2015-04-22 |
| Phase | Phase 3 |
What the finished NCT00418262 record still lists
NCT00418262 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 27 participants, a relatively small participant target, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (97% lower).
The record links to 0 conditions, and to 1 intervention - of which Atomoxetine is the first listed.
NCT00418262 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00418262 about?
NCT00418262 is a clinical study titled "Open-Label Study of the Long Term Tolerability and Safety of Atomoxetine in Children With FASD and ADD/ADHD". Determine if atomoxetine is safe and well tolerated by children with fetal alcohol syndrome.
What is the current status of trial NCT00418262?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 27 participants. The study started on 2005-08. Estimated completion is 2015-04-22.
What interventions are being tested in trial NCT00418262?
The interventions under investigation include: Atomoxetine (DRUG).
Who is sponsoring clinical trial NCT00418262?
This trial is sponsored by University of Oklahoma, which has 358 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00418262's enrollment target sits among peer trials
27 1936th of 2000 higher than 64 of 2,000 other Phase 3 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 3 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
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT00912041 · 27 participants · NA
BrainGate2: Feasibility Study of an Intracortical Neural Interface System for Persons With Tetraplegia
- NCT02847559 · 27 participants · Phase 2
Optune Delivered Electric Field Therapy and Bevacizumab in Treating Patients With Recurrent or Progressive Grade 2 or 3 Meningioma
- NCT03380195 · 27 participants · NA
Effects of Watermelon Juice on Heart Rate Recovery and Post-exercise Muscle Soreness
- NCT03384238 · 27 participants · Phase 1
Panitumumab-IRDye800 in Patients With Pancreatic Cancer Undergoing Surgery
Similar registry start date
- NCT05988463 · started 2027-01-01 · Phase 1
Dose-Escalation Study of Artesunate Patients With IPF
- NCT07219706 · started 2026-12-10 · NA
Dietary Fiber and Time Restricted Eating
- NCT02831335 · started 2026-12-01
Technical Development of Multi-Parametric Renocerebral MRI
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia