drugset / Trial / NCT00269776

An Effectiveness and Safety Study Evaluating OROS Methylphenidate Hydrochloride (HCl), Ritalin (Methylphenidate HCl) and Placebo in Children With Attention Deficit Hyperactivity Disorder

NCT00269776

Phase 3 Completed Alza Corporation
RandomizedCrossoverQuadruple-blindTreatment

Summary

The purpose of this study is to provide data on the effectiveness of the OROS Methylphenidate Hydrochloride (HCl) formulation compared to placebo and standard immediate-release Ritalin with respect to improving attention and behavior, and decreasing hyperactivity in children with Attention Deficit Hyperactivity Disorder (ADHD). Both OROS Methylphenidate HCl and Ritalin contain the central nervous system stimulant, methylphenidate HCl. The safety associated with the two methylphenidate formulations will also be compared with placebo.

Timeline

Start
1998-11
Primary completion
Completion
1999-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Methylphenidate Small molecule 5 mg Oral
Subject Methylphenidate Small molecule 10 mg Oral
Subject Methylphenidate Small molecule 15 mg Oral
Subject Methylphenidate Small molecule 18 mg Oral
Subject Methylphenidate Small molecule 36 mg Oral
Subject Methylphenidate Small molecule 54 mg Oral