drugset / Trial / NCT00518232

A Study to Determine Effective and Tolerable Titration Scheme for OROS-Methylphenidate in Children With Attention-deficit Hyperactivity Disorder

NCT00518232 ↗

Phase 4 Completed 520 enrolled Johnson & Johnson Taiwan Ltd
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of the study is to investigate the clinical benefit of switching children with ADHD from immediate-release methylphenidate (IR-MPH) to OROS-methylphenidate under the correct dosage conversion scheme.

Timeline

Start
2006-09
Primary completion
2007-06
Completion
2007-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Methylphenidate Small molecule 18 mg —
Subject Methylphenidate Small molecule 36 mg —
Subject Methylphenidate Small molecule 54 mg —