Clinical trial

Efficacy of Atomoxetine on Psychosocial Function of Children and Adolescents…

NCT00320528 · Eli Lilly and Company, Industry · Completed

Key facts

NCT number NCT00320528
Title Efficacy of Atomoxetine on Psychosocial Function of Children and Adolescents With Attention-Deficit/Hyperactivity Disorder (ADHD)
Official title An Open-Label Study of the Efficacy of Atomoxetine Hydrochloride on Quality of Life of Children and Adolescents With Attention-Deficit/Hyperactivity Disorder With or Without Comorbid Conditions
Lead sponsor Eli Lilly and Company, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Attention Deficit Disorder With Hyperactivity
Intervention type Drug
Interventions atomoxetine
Enrollment 269
Start date Apr 1, 2006
Primary completion Oct 1, 2008
Completion Oct 1, 2008
First posted May 3, 2006
Last update posted Jan 6, 2010
Countries Italy

At a glance

  • 10–99 Study sites
  • 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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