CompletedNCT00962104
Atomoxetine to Treat Asian Adult Patients With Attention-Deficit/Hyperactivity Disorder
Medication studyAges 18+Multiple countriesADHD
Understand this study
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 23 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
Study start dateAugust 2009
- Recruitment status
- Completed
- Enrollment listed in the registry
- 391
- 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, South Korea, Taiwan
- Age range
- Over 18 Years
- Official registry ID
- NCT00962104
- Official title
Show the full official title
A Double-Blind Placebo-Controlled Asian Study of Atomoxetine Hydrochloride in the Treatment of Adult Patients With Attention-Deficit/Hyperactivity Disorder (ADHD)
Recruitment & locations
CompletedAichi, Japan · Chiba, Japan · Fukushima, Japan
21 more locations
- Hokkaido, Japan
- Hyōgo, Japan
- Kanagawa, Japan
- Kumamoto, Japan
- Kyoto, Japan
- Nara, Japan
- Osaka, Japan
- Saitama, Japan
- Tokyo, Japan
- Bucheon-si, South Korea
- Gwangjin-Gu, South Korea
- Jeonju, South Korea
- Seoul, South Korea
- Sungnam-Si, South Korea
- Yangsan, South Korea
- Keelung, Taiwan
- Neihu Taipei, Taiwan
- Niao Sung Hsiang, Taiwan
- Taichung, Taiwan
- Taipei, Taiwan
- Taoyuan, Taiwan
Questions about this study
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 and Placebo.
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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