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CompletedNCT00937040

OROS methylphenidate for adults with ADHD

About this title

Read the official source —
Medication studyAges 18–65
The study in practice

Understand this study

Who was this study for?

Listed age limits: 18 years to 65 years.

Study phase
Phase 4Usually happens after approval, to monitor real-world use, safety, and longer-term outcomes.
Study clarity

Study information

Study start dateJuly 2009
Recruitment status
Completed
Enrollment listed in the registry
357
Sponsor
Ortho-McNeil Janssen Scientific Affairs, LLC
Sponsor type
Other organization
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 4Usually happens after approval, to monitor real-world use, safety, and longer-term outcomes.
Locations
Not clearly listed
Age range
From 18 Years to 65 Years
Official registry ID
NCT00937040
Official title
Show the full official title

A Placebo Controlled Double-Blind, Parallel Group, Individualizing Dosing Study Optimizing Treatment of Adults With Attention Deficit Hyperactivity Disorder to an Effective Response With OROS Methylphenidate

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Recruitment & locations

Completed

Locations not listed

FAQ

Questions about this study

Who is behind this study?

The study sponsor is Ortho-McNeil Janssen Scientific Affairs, LLC.

Did this study involve medication?

Yes. The study involved medication, including OROS MPH, Placebo, OROS MPH Tablets and Placebo Tablets.

Who was this study for?

Listed age limits: 18 years to 65 years.

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