A Comparative Effectiveness Study Evaluating OROS Methylphenidate HCl, Ritalin (Methylphenidate HCl), and Placebo for the Treatment of Attention Deficit Hyperactivity Disorder in Children

Last updated: June 9, 2011
Sponsor: Alza Corporation, DE, USA
Overall Status: Completed

Phase

3

Condition

Attention Deficit/hyperactivity Disorder (Adhd - Adults)

Autism Spectrum Disorder (Asd)

Williams Syndrome

Treatment

N/A

Clinical Study ID

NCT00269789
CR005992
  • Ages 6-12
  • All Genders

Study Summary

The purpose of this study is to compare the effectiveness (onset of effect, time to loss of effect, and overall efficacy) of methylphenidate given as an OROS® (methylphenidate HCl) formulation, compared to immediate-release Ritalin® and placebo for the treatment of Attention Deficit Hyperactivity Disorder (ADHD) in children using standardized attention and behavior scales, and other assessments. Both OROS® Methylphenidate HCl and Ritalin® contain the central nervous system stimulant, methylphenidate HCl.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Patients with a diagnosis of one of the three subtypes of Attention DeficitHyperactivity Disorder (ADHD) verified by both a parent/child interview and a teacherassessment using SNAP-IV questionnaires

  • taking 5 - 20 mg of immediate-release methylphenidate (Ritalin®) at least twice a day, 20 - 60 mg of sustained-release methylphenidate (Ritalin-SR®) per day, or acombination of immediate-release and sustained-release methylphenidate up to a dailydose not exceeding 60 mg

  • having used methylphenidate for at least 3 months at some time in the past and havebeen on the same dose for the previous 4-week period without any significant adverseexperiences, considered to be positive responders to methylphenidate therapy, andagreeing to take only the supplied study drug as treatment for ADHD during thethree-week treatment phase of the study

  • able to comply with the study visit schedule and whose parent(s) and teacher arewilling and able to complete the protocol-specified assessments, including behaviormodification procedures

  • agreeing not to ingest any caffeine containing beverages (e.g., coffee or soda) orfoods (e.g., chocolate) on days 7, 14, and 21 of the study

Exclusion

Exclusion Criteria:

  • Patients having clinically significant gastrointestinal problems, including narrowingof the gastrointestinal tract

  • considered markedly anxious, tense, agitated, or depressed, having psychoticdisorders, a history of seizures, or having a diagnosis of Tourette's syndrome

  • whose primary treatment focus is oppositional-defiant disorder, conduct disorder, ortics, or whose primary treatment focus is other psychiatric conditions such asdepressive disorders, bipolar disorders, or other mood disorders

  • having a mean of two blood pressure measurements (systolic or diastolic) equal to orgreater than the 95th percentile for age, sex, and height

  • if female, have begun menstruation

Study Design

Study Start date:
March 01, 1998
Estimated Completion Date:
May 31, 1998

Study Description

Attention Deficit Hyperactivity Disorder (ADHD) represents the most common neurobehavioral disorder in children, affecting 3% to 5% of the school-age population. This is a double-blind, double-dummy, randomized, placebo-controlled, active-controlled, crossover trial in children with ADHD, to compare the safety and effectiveness (onset of effect, time to loss of effect and overall efficacy) of OROS® Methylphenidate HCl with standard immediate-release Ritalin® and placebo. During this study, patients receive each of the three treatments (OROS® Methylphenidate HCl 18, 36 or 54 milligrams per day, Ritalin® 5, 10 or 15 milligrams three times per day, or placebo) for 7 days, and are assigned to one of three dosage levels depending upon their prestudy methylphenidate dose and regimen. The total study participation for each patient will be 21 days. Since ADHD is manifested in a variety of settings and can affect attention and behavior, this study assesses efficacy in home, community school, and laboratory school settings using numerous assessments designed to evaluate various aspects of the disorder. These assessments are completed by a variety of raters, including the parents/caregivers, community school teachers, laboratory school teachers and the laboratory school counselor. The primary measure of effectiveness is the community school teacher's rating on the IOWA Conners Inattention/Overactivity subscale. Additional measures of effectiveness include IOWA Conners (Inattention/Overactivity and Oppositional/Defiance subscale) ratings, SKAMP attention and deportment ratings, peer interaction and other behavioral ratings, global assessments, accuracy and productivity of independent assigned academic seatwork, and assessments of positive and negative social behaviors, classroom rule violations and disruptive behaviors. Safety evaluations include the incidence of adverse events, vital signs, sleep quality, appetite, and the presence/severity of tics (hard-to-control, repeated twitching of any parts of the body or hard-to-control repeating of sounds or words). Patients will be given oral doses of: OROS® (methylphenidate HCl) either 1, 2 or 3 of the 18 milligram tablets once daily, Ritalin® 5, 10, or 15 mg (encapsulated/single capsule) three times per day, or placebo. There are three treatment groups, each group dosing for 7 days for a total of 21 days on study.