drugset / Trial / NCT00141063

Safety and Efficacy Study of Dexmethylphenidate in Children With ADHD

NCT00141063

Phase 3 Completed 90 enrolled Novartis
RandomizedCrossoverDouble-blindTreatment

Summary

The purpose of this study is to compare the safety and efficacy of two doses of dexmethylphenidate to two doses of an approved, long-acting, marketed medication for ADHD (MPH) and placebo in children ages 6-12 diagnosed with ADHD.

Timeline

Start
2005-06
Primary completion
Completion
2005-08

Drugs

EvaluationDrugModalityDoseRoute
Subject dexmethylphenidate Unknown