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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 Adol...

Mise à jour : Il y a 4 ans
Référence : EUCTR2008-001767-11

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)

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Extrait

The primary objective of the study is to compare the efficacy of 2 different switching approaches; at the end of the fast (Week 2) and slow (Week 10) transition from stimulants to atomoxetine as measured by Attention-Deficit/Hyperactivity Disorder Rating Scale-Parent Version: Investigator-Administered and Scored (ADHD-RS-IV Parent: Inv). The analysis will be based on the change from baseline to Weeks 2 and 10, respectively.

Critère d'inclusion

  • Attention-Deficit/Hyperactivity Disorder (ADHD)

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