Memantine for Executive Dysfunction in Adults With ADHD: A Pilot Study

NACompletedINTERVENTIONAL
Enrollment

33

Participants

Timeline

Start Date

May 31, 2012

Primary Completion Date

July 31, 2013

Study Completion Date

August 31, 2013

Conditions
Attention Deficit Hyperactivity Disorder (ADHD)Executive Function Deficits (EFD)
Interventions
DRUG

Placebo

Memantine-matched placebo will be prescribed following approved FDA dosing guidelines for Alzheimer's dementia, beginning at 5mg in AM and increasing in BID doses by 5mg weekly to a maximum dose of 10mg BID.

DRUG

Memantine Hydrochloride

Memantine will be prescribed following approved FDA dosing guidelines for Alzheimer's dementia, beginning at 5mg in AM and increasing in BID doses by 5mg weekly to a maximum dose of 10mg BID.

DRUG

OROS-Methylphenidate

OROS-Methylphenidate will be openly prescribed, starting with an initial dose of 36mg/day and titrated to optimal response to a maximum daily dose of 1.3mg/kg or 108mg/day, whichever is lower, according to clinician judgment. During titration, dose will be increased on a weekly basis in 36mg/day increments. The dose may be reduced by 18 or 36mg/day increments if adverse effects occur or if the subject discontinues treatment.

Trial Locations (1)

02114

Massachusetts General Hospital, Boston

All Listed Sponsors
collaborator

The American Professional Society of ADHD and Related Disorders (APSARD)

UNKNOWN

lead

Massachusetts General Hospital

OTHER

NCT01533493 - Memantine for Executive Dysfunction in Adults With ADHD: A Pilot Study | Biotech Hunter | Biotech Hunter