Expired Study
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Houston, Texas 77007


Purpose:

The purpose of this study is to compare the safety and efficacy of two doses of dexmethylphenidate to two doses of an approved, long-acting, marketed medication for ADHD (MPH) and placebo in children ages 6-12 diagnosed with ADHD.


Criteria:

Inclusion Criteria: - DSM-IV diagnosis of ADHD - Males and females aged 6-12 Exclusion Criteria: - Inability to understand or follow instructions - Is pregnant - Diagnosis of tic disorder - History of seizure disorder


NCT ID:

NCT00141050


Primary Contact:

Principal Investigator
Matthew Brams, MD
Bayou City Research


Backup Contact:

N/A


Location Contact:

Houston, Texas 77007
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: December 17, 2017

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