Memantine Monotherapy for Executive Dysfunction and ADHD



Status:Not yet recruiting
Conditions:Psychiatric, ADHD
Therapuetic Areas:Psychiatry / Psychology, Other
Healthy:No
Age Range:18 - 45
Updated:10/3/2013
Start Date:July 2013

Use our guide to learn which trials are right for you!

Memantine Monotherapy for Executive Dysfunction and ADHD: A Pilot Study


This is a 12-week clinical trial evaluating the efficacy and safety of memantine
hydrochloride (Memantine HC1, brand name Namenda) in the treatment of executive function
deficits (EFDs) in adults with Attention Deficit Hyperactivity Disorder (ADHD). After
screening procedures, memantine is prescribed in randomized, double-blind fashion (equal
chance of medication or placebo) for 12 weeks.

The investigators hypothesize that memantine hydrochloride will prove to be an effective,
safe, and well-tolerated agent for the treatment of EFDs in individuals with ADHD interested
in non-stimulant medications.


Inclusion Criteria:

1. Male and female adults ages 18-45 years;

2. a diagnosis of DSM-IV [78] ADHD-combined type

3. a score of at least 20 on the AISRS (a score of 20 in the AISRS identifies subjects
with at least moderate severity of symptoms);

4. a BRIEF-A Global Executive Composite T-score of >6; and

5. proficiency in English. -

Exclusion Criteria:

1) Pregnant or nursing females; 2) investigator and his/her immediate family (spouse,
parent, child, grandparent, or grandchild); 3) any serious, unstable medical illness
including hepatic, renal, gastroenterological, respiratory, cardiovascular (including
ischemic heart disease and hypertension), endocrinologic, neurologic, immunologic, or
hematologic disease; 4) hypersensitivity to memantine; 5) multiple adverse drug reactions;
6) current or past history of seizures; 7) any history of a major psychiatric disorder
including schizophrenia, psychosis, bipolar disorder (BPD), or autism spectrum disorder
(ASD); 8) meets DSM-IV criteria in the last month for major depression or any major
anxiety disorder or has a Hamilton Rating Scale for Anxiety (HAM-A) or Hamilton Rating
Scale for Depression (HAM-D) score greater than 14; 9) meets DSM-IV criteria for substance
abuse or dependence in the last month or has a positive drug urine screen; 10) judged to
be at serious suicidal risk; 11) use of any other concomitant medication with primarily
central nervous system activity; or 12) IQ < 80.

-
We found this trial at
1
site
185 Cambridge Street
Boston, Massachusetts 02114
617-724-5200
?
mi
from
Boston, MA
Click here to add this to my saved trials