Clinical trial

Characterization of Dermal Reactions in Pediatric Patients With ADHD Using…

NCT00434213 · Noven Therapeutics, Industry · Completed

Key facts

NCT number NCT00434213
Title Characterization of Dermal Reactions in Pediatric Patients With ADHD Using DAYTRANA
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).
Lead sponsor Noven Therapeutics, Industry
Status Completed
Phase Phase 4
Study type Interventional
Conditions Attention Deficit Hyperactivity Disorder
Intervention type Drug
Interventions Daytrana
Enrollment 309
Start date Jan 1, 2007
Primary completion Aug 1, 2007
Completion Jul 1, 2008
First posted Feb 13, 2007
Last update posted Apr 26, 2017
Countries United States

At a glance

  • Yes Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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