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CompletedNCT00304681

Concerta or immediate-release methylphenidate for after-school ADHD symptoms

About this titleRead the official source — NCT00304681
Medication studyAges 6–12
The study in practice

Understand this study

Who was this study for?

Listed age limits: 6 years to 12 years.

Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.

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Study clarity

Study information

Study start dateNot clearly listed
Recruitment status
Completed
Enrollment listed in the registry
147
Sponsor
Janssen-Ortho Inc., Canada
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
Not clearly listed
Age range
From 6 Years to 12 Years
Official registry ID
NCT00304681
Official title
Show the full official title

The Effectiveness of CONCERTA® vs. Usual Clinical Care With Immediate Release Methylphenidate (IR MPH) in Children (6-12 Years) With Attention Deficit Hyperactivity Disorder (ADHD): A Randomized, Open-Label Trial

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Recruitment & locations

Completed

Locations not listed

FAQ

Questions about this study

Who is behind this study?

The study sponsor is Janssen-Ortho Inc., Canada.

Did this study involve medication?

Yes. The study involved medication, including OROS*-Methylphenidate.

Who was this study for?

Listed age limits: 6 years to 12 years.

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