Atomoxetine Pilot Study in Preschool Children With ADHD

PHASE4CompletedINTERVENTIONAL
Enrollment

31

Participants

Timeline

Start Date

April 30, 2004

Primary Completion Date

March 31, 2008

Conditions
Attention Deficit Hyperactivity Disorder
Interventions
DRUG

ATMX

Medication phase: After screening assessments are completed, the child will enter the medication phase of the study. The child will be started on atomoxetine at 0.5 mg/kg/day, with the dosage increased to a maximum dose of 1.8 mg/kg/day. The dose will be determined by how well the child responds to and tolerates the drug. The dose will be given twice a day to minimize side effects. After the optimum dose is determined, the child will be kept at this stable dose for 4 weeks.

Trial Locations (1)

85724

University of Arizona Department of Psychiatry, Tucson

All Listed Sponsors
lead

University of Arizona

OTHER

NCT00517647 - Atomoxetine Pilot Study in Preschool Children With ADHD | Biotech Hunter | Biotech Hunter