Clinical trial

A Study Comparing the Effect of Atomoxetine Versus Other Standard Care Therapy…

NCT00447278 · Eli Lilly and Company, Industry · Completed

Key facts

NCT number NCT00447278
Title A Study Comparing the Effect of Atomoxetine Versus Other Standard Care Therapy on the Long Term Functioning in Attention-Deficit/Hyperactivity Disorder (ADHD) Children and Adolescents
Official title A Randomized, Controlled, Open-Label Study of the Long-Term Impact on Functioning Using Atomoxetine Hydrochloride Compared to Other Early Standard Care in the Treatment of Attention-Deficit/Hyperactivity Disorder in Treatment-Naïve Children and Adolescents
Acronym ADHD LIFE
Lead sponsor Eli Lilly and Company, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Attention Deficit Hyperactivity Disorder
Intervention type Drug
Interventions Atomoxetine, Other standard therapy for ADHD
Enrollment 399
Start date Mar 1, 2007
Primary completion Mar 1, 2009
Completion Jul 1, 2009
First posted Mar 14, 2007
Last update posted Apr 27, 2010
Countries Belgium, France, Ireland, Italy, Mexico, Norway, Spain, Turkey (Türkiye), United Kingdom

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.

About ClinicalTrials.gov studies

ClinicalTrials.gov is the U.S. National Library of Medicine's registry of clinical studies conducted around the world. Contact and investigator details are not shown here.

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

Browse all ClinicalTrials.gov studies