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Clinical trial

A Randomized, Controlled, Open-Label Comparison Study of the Efficacy and Safety of Slow Transitioning Compared With Fast Transitioning From a Stimulant Medication to Atomoxetine in Pediatric and Adolescent Outpatients With DSM-IV Attention-Deficit/Hyperactivity Disorder (ADHD)

NCT00760747 is registered in ClinicalTrials.gov with Eli Lilly and Company as lead sponsor.

NCT NCT00760747
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Registry record

As filed in ClinicalTrials.gov.

Title
A Randomized, Controlled, Open-Label Comparison Study of the Efficacy and Safety of Slow Transitioning Compared With Fast Transitioning From a Stimulant Medication to Atomoxetine in Pediatric and Adolescent Outpatients With DSM-IV Attention-Deficit/Hyperactivity Disorder (ADHD)
Lead sponsor
Eli Lilly and Company
Phase
Phase 4
Overall status
Completed
Start date
September 30, 2008
Completion date
September 30, 2010
Enrollment
112 (actual)
Sites
6

Conditions

As the registry lists them; a condition with its own page is linked.

attention deficit hyperactivity disorder