drugset / Trial / NCT00931398

Treatment of College Students With Attention-Deficit/Hyperactivity Disorder (ADHD) Using OROS Methylphenidate

NCT00931398 ↗

RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of the proposed study is to determine the effectiveness of methylphenidate HCl (Concerta) in college students with ADHD. This study will consist of 110 college students between the ages of 18 and 25 who are enrolled full-time in a local or junior college. The study consists of an 8-week double-blind, placebo-controlled trial of placebo versus methylphenidate HCl (Concerta®) followed by a 10-week extension of open label methylphenidate HCl (Concerta®).

Timeline

Start
2010-04
Primary completion
2010-04
Completion
2010-04

Outcome

Outcome not reported

Stopped (Business): “Study was not initiated due to lack of funding by the sponsor”

Drugs

EvaluationDrugModalityDoseRoute
Subject Methylphenidate Small molecule 18 mg —
Subject Methylphenidate Small molecule 36 mg —
Subject Methylphenidate Small molecule 54 mg —
Subject Methylphenidate Small molecule 72 mg —