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CompletedNCT00434213

Skin reactions to methylphenidate patches in children with ADHD

About this titleRead the official source — NCT00434213
Medication studyAges 6–12United States
The study in practice

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Who was this study for?

Listed age limits: 6 years to 12 years.

Listed locations
Scottsdale and 28 more locationsSee all locations and recruitment
Study phase
Phase 4Usually happens after approval, to monitor real-world use, safety, and longer-term outcomes.

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Study clarity

Study information

Study start dateJanuary 2007
Recruitment status
Completed
Enrollment listed in the registry
309
Sponsor
Noven Therapeutics
Sponsor type
Biotech company
Study type
Drug
Intervention type
Drug
Study phase
Phase 4Usually happens after approval, to monitor real-world use, safety, and longer-term outcomes.
Locations
United States
Age range
From 6 Years to 12 Years
Official registry ID
NCT00434213
Official title
Show the full official title

A Phase IV, Multi-center, Open-label Study of DAYTRANA (Methylphenidate Transdermal System [MTS]) to Characterize the Dermal Reactions in Pediatric Patients Aged 6-12 With Attention Deficit/Hyperactivity Disorder (ADHD).

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Recruitment & locations

Completed

Scottsdale · Irvine · San Marcos

26 more locations
  • Spring Valley
  • Wildomar
  • Boulder
  • Gainesville
  • Miami
  • Winter Park
  • Libertyville
  • Northbrook
  • Overland Park
  • Bardstown
  • Owensboro
  • Cambridge
  • Kalamazoo
  • Las Vegas
  • Toms River
  • Rochester
  • Cleveland
  • Columbus
  • Portland
  • Salem
  • Philadelphia
  • Jackson
  • Austin
  • Lubbock
  • San Antonio
  • Norfolk

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FAQ

Questions about this study

Who is behind this study?

The study sponsor is Noven Therapeutics.

Did this study involve medication?

Yes. The study involved medication, including Daytrana.

Who was this study for?

Listed age limits: 6 years to 12 years.

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