drugset / Trial / NCT00776009

Efficacy and Safety of Dex-Methylphenidate Extended Release 30 mg Versus 20 mg in Children (6-12 Years) With Attention-Deficit/Hyperactivity Disorder (ADHD) in a Laboratory Classroom Setting.

NCT00776009 ↗

Phase 4 Completed 165 enrolled Novartis Pharmaceuticals
RandomizedCrossoverQuadruple-blindTreatment

Summary

This study will evaluate the efficacy and safety of Dex-Methylphenidate Extended Release 30 mg compared to 20 mg in pediatric patients ages 6-12 with Attention-Deficit Hyperactivity Disorder (ADHD) in a 12-hour laboratory classroom setting.

Timeline

Start
2008-10
Primary completion
2008-12
Completion
2008-12

Outcome

Met primary endpoint

paper Mean Avg (10-12) change from pre-dose [corrected] in SKAMP-Combined score was significantly greater for D-MPH-ER 30 mg (-4.47) compared with D-MPH-ER 20 mg (-2.02; P = 0.002). PMID 22926597 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject dexmethylphenidate Unknown 20 mg —
Subject dexmethylphenidate Unknown 30 mg —