An fMRI Study of Stimulant vs. Non-Stimulant Treatment of ADHD

NATerminatedINTERVENTIONAL
Enrollment

38

Participants

Timeline

Start Date

September 30, 2014

Primary Completion Date

November 6, 2021

Study Completion Date

November 6, 2021

Conditions
Attention Deficit Hyperactivity Disorder
Interventions
DRUG

Guanfacine

Participants will meet with the study doctor on a weekly basis during the treatment phase of the study. In the first few weeks, the daily dose of the medication will be individually adjusted by the study doctor according to participants' clinical response to and tolerability of the medication. The optimal dose will then be maintained for the remainder of the treatment period.

DRUG

Lisdexamfetamine

Participants will meet with the study doctor on a weekly basis during the treatment phase of the study. In the first few weeks, the daily dose of the medication will be individually adjusted by the study doctor according to participants' clinical response to and tolerability of the medication. The optimal dose will then be maintained for the remainder of the treatment period.

Trial Locations (1)

10032

New York State Psychiatric Institute, New York

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Columbia University

OTHER

collaborator

American Academy of Child Adolescent Psychiatry.

OTHER

collaborator

Shire

INDUSTRY

lead

New York State Psychiatric Institute

OTHER