Safety study of Long-term Safety and Efficacy of ORADUR®-Methylphenidate in ADHD
Researchers studied ORADUR-Methylphenidate, tracking side effects to assess long-term safety in children and adolescents with ADHD.
Understand this study
What did researchers investigate?
Researchers studied ORADUR-Methylphenidate, tracking side effects to assess long-term safety in children and adolescents with ADHD.
Who was this study for?
This study was for people with ADHD. Listed age limits: 6 years to 18 years. Other eligibility criteria applied.
- Listed locations
- Chiayi City, Taiwan · Taipei, Taiwan and 1 more locationSee all locations and recruitment
- Activities
- Medication described in the protocol
- Compensation
- Payment and expense reimbursement have not been verified.
Study information
- Recruitment status
- Completed
- Enrollment listed in the registry
- 64
- Sponsor
- Orient Pharma Co., Ltd.
- Sponsor type
- Pharmaceutical company
- 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
- Taiwan
- Age range
- From 6 Years to 18 Years
- Official registry ID
- NCT02704390
- Official title
Show the full official title
An Extension Study to Evaluate the Long-term Safety and Efficacy of ORADUR®-Methylphenidate in Children and Adolescents With ADHD
Recruitment & locations
CompletedChiayi City · Taipei · Taoyuan
Questions about this study
What did researchers investigate?
Researchers studied ORADUR-Methylphenidate, tracking side effects to assess long-term safety in children and adolescents with ADHD.
Who is behind this study?
The study sponsor is Orient Pharma Co., Ltd., a pharmaceutical company.
Did this study involve medication?
Yes. The study involved medication, including ORADUR®-Methylphenidate.
Who was this study for?
This study was for people with ADHD. Listed age limits: 6 years to 18 years. Other eligibility criteria applied.
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