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Completed Phase 3 Interventional

Safety & Tolerability of MTS in Children Aged 6-12 Diagnosed With ADHD & Previously Treated With Extended-Release Methylphenidate Therapy

ClinicalTrials.gov ID: NCT00151983

Public ClinicalTrials.gov record NCT00151983. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 5:43 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Prospective, Open-Label, Multi-Center Study Evaluating the Safety and Tolerability of Methylphenidate Transdermal System (MTS) in Children Aged 6-12 Previously Treated With Extended-Release Methylphenidate Product.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study will assess the safety and tolerability of MTS while attempting to establish the appropriate starting dose for subjects previously on an existing long-acting methylphenidate product.

Study identification

NCT ID
NCT00151983
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Noven Therapeutics
Industry
Enrollment
175 participants

Conditions and interventions

Eligibility (public fields only)

Age range
6 Years to 12 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 2005 (Type not available)
Primary completion
Jul 2006 (Actual)
Completion
Jul 2006 (Actual)
Last update posted
Jul 9, 2015

2005 – 2006

United States locations

U.S. sites
18
U.S. states
15
U.S. cities
18
Facility City State ZIP Site status
Meadowbrook Research, Inc. Scottsdale Arizona — —
Psychiatric Centers at San Diego San Marcos California — —
Alpine Clinical Research Center Boulder Colorado — —
Miami Research Associates, Inc. Miami Florida — —
Capstone Clinical Research Libertyville Illinois — —
Pedia Research, LLC Owensboro Kentucky — —
ProMed Pediatrics Kalamazoo Michigan — —
Children's Specialized Hospital Toms River New Jersey — —
North Carolina Neuropsychiatry PA Chapel Hill North Carolina — —
Ohio State University Columbus Ohio — —
IPS Research Company Oklahoma City Oklahoma — —
Oregon Center for Clinical Investigations (OCCI, Inc.) Portland Oregon — —
CNS Research Institute Philadelphia Pennsylvania — —
Western Psychiatric Institute & Clinic Pittsburgh Pennsylvania — —
Claghorn-Lesem Research Clinic Bellaire Texas — —
ADHD Clinic of San Antonio San Antonio Texas — —
NeuroScience, Inc. Herndon Virginia — —
Monarch Medical Research Norfolk Virginia — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00151983, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 9, 2015 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00151983 live on ClinicalTrials.gov.

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