A Long Term Follow-Up Study for Asian Adult Patients With Attention Deficit Hyperactivity Disorder
Researchers studied atomoxetine, tracking side effects to assess long-term safety and tolerability in adults with ADHD.
Understand this study
What did researchers investigate?
Researchers studied atomoxetine, tracking side effects to assess long-term safety and tolerability in adults with ADHD.
Who was this study for?
This study was for people with ADHD. Listed age limits: from 18 years. Other eligibility criteria applied.
- Listed locations
- Aichi and 11 more locationsSee all locations and recruitment
- Study phase
- Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
Study information
- Recruitment status
- Completed
- Enrollment listed in the registry
- 211
- Sponsor
- Eli Lilly and Company
- Sponsor type
- Other organization
- Study type
- Drug
- Intervention type
- Medication / drug
- Study phase
- Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
- Locations
- Japan
- Age range
- Over 18 Years
- Official registry ID
- NCT00969618
- Official title
Show the full official title
Long-Term, Open-Label Safety and Efficacy Study of Atomoxetine Hydrochloride in Adult Patients With Attention-Deficit/Hyperactivity Disorder (ADHD)
Recruitment & locations
CompletedAichi · Chiba · Fukushima
9 more locations
- Hokkaido
- Hyōgo
- Kanagawa
- Kumamoto
- Kyoto
- Nara
- Osaka
- Saitama
- Tokyo
Questions about this study
What did researchers investigate?
Researchers studied atomoxetine, tracking side effects to assess long-term safety and tolerability in adults with ADHD.
Who is behind this study?
The study sponsor is Eli Lilly and Company.
Did this study involve medication?
Yes. The study involved medication, including Atomoxetine.
Who was this study for?
This study was for people with ADHD. Listed age limits: from 18 years. Other eligibility criteria applied.
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