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Completed Phase 4 Interventional Results available

Characterization of Dermal Reactions in Pediatric Patients With ADHD Using DAYTRANA

ClinicalTrials.gov ID: NCT00434213

Public ClinicalTrials.gov record NCT00434213. 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 Sep 5, 2026, 8:59 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 Phase IV, Multi-center, Open-label Study of DAYTRANA (Methylphenidate Transdermal System [MTS]) to Characterize the Dermal Reactions in Pediatric Patients Aged 6-12 With Attention Deficit/Hyperactivity Disorder (ADHD).

Brief summary

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

This is a study designed to characterize the dermal response of DAYTRANA. Subjects will visit the study site over a period of approximately 14 weeks.

Study identification

NCT ID
NCT00434213
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Noven Therapeutics
Industry
Enrollment
309 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
Dec 31, 2006
Primary completion
Jul 31, 2007
Completion
Jun 30, 2008
Last update posted
Apr 25, 2017

2007 – 2008

United States locations

U.S. sites
29
U.S. states
18
U.S. cities
29
Facility City State ZIP Site status
Not listed Scottsdale Arizona
Not listed Irvine California
Not listed San Marcos California
Not listed Spring Valley California
Not listed Wildomar California
Not listed Boulder Colorado
Not listed Gainesville Florida
Not listed Miami Florida
Not listed Winter Park Florida
Not listed Libertyville Illinois
Not listed Northbrook Illinois
Not listed Overland Park Kansas
Not listed Bardstown Kentucky
Not listed Owensboro Kentucky
Not listed Cambridge Massachusetts
Not listed Kalamazoo Michigan
Not listed Las Vegas Nevada
Not listed Toms River New Jersey
Not listed Rochester New York
Not listed Cleveland Ohio
Not listed Columbus Ohio
Not listed Portland Oregon
Not listed Salem Oregon
Not listed Philadelphia Pennsylvania
Not listed Jackson Tennessee
Not listed Austin Texas
Not listed Lubbock Texas 79423
Not listed San Antonio Texas
Not listed 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 NCT00434213, 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 Apr 25, 2017 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00434213 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →