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Search / Trial NCT00414921

Preschool Supplement to Clonidine in ADHD (Kiddie-CAT)

Launched by UNIVERSITY OF CINCINNATI · Dec 21, 2006

Trial Information

Current as of August 27, 2025

Completed

Keywords

Attention Deficit Hyperactivity Disorder Adhd Clonidine Methylphenidate Mph

ClinConnect Summary

Attention deficit hyperactivity disorder (ADHD) is a disease characterized by one or more symptoms of hyperactivity, impulsivity, or inattention that interfere with school, home, work, or social settings. ADHD does not have clear physical signs that can be seen in an x-ray or a lab test. The disorder only can be identified by looking for certain behaviors, which vary from person to person.

This trial will compare the benefits and side effects of two medications--clonidine and methylphenidate (MPH)--used alone or in combination to treat ADHD in children. MPH is approved by the Food and Drug...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Child with ADHD
  • Child ages 4 through 6
  • Child attending a structured preschool or daycare
  • Exclusion Criteria:
  • Presence of a tic disorder of any kind or a known active heart disease for which it would be unsafe to use the study drugs
  • Presence of pervasive developmental disorder, autism, mental retardation, or serious psychiatric illness
  • Child not attending a structured preschool or daycare

About University Of Cincinnati

The University of Cincinnati is a leading research institution dedicated to advancing healthcare through innovative clinical trials and studies. With a robust focus on translational research, the university fosters a collaborative environment that integrates cutting-edge science with clinical practice. Its diverse team of experts, equipped with state-of-the-art facilities, is committed to exploring new therapeutic interventions aimed at improving patient outcomes. The University of Cincinnati actively engages in partnerships with industry and academia to drive forward-thinking solutions in medicine, ensuring that research findings are effectively translated into real-world applications.

Locations

Rochester, New York, United States

Cincinnati, Ohio, United States

Pittsburgh, Pennsylvania, United States

Patients applied

0 patients applied

Trial Officials

Floyd Randy Sallee, MD/PhD

Principal Investigator

University of Cincinnati

Oscar Bukstein, MD

Principal Investigator

Western Psychiatric Institute and Clinic

Donna Palumbo, PhD

Principal Investigator

University of Rochester

William Pelham, PhD

Principal Investigator

SUNY Buffalo

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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