Abstract | OBJECTIVE: METHOD: This was a 12-week, double-blind, placebo-controlled, randomized clinical trial of memantine added to open-label treatment with stimulant medication. Because of the small sample size, we considered a standardized mean difference (equivalent to effect size) of ≥0.5 and odds ratios ≥2 as indicators of trend improvements. RESULTS: Twelve participants received memantine and 14 received a placebo. Trend improvements favoring memantine were observed on Behavior Rating Inventory of Executive Functions-Adult Inhibition and Self-Monitor subscales when compared with Placebo. No significant changes were noted on the Cambridge Neuropsychological Test Automated Battery. CONCLUSION: Among adults with ADHD and EFDs, adjunct treatment with memantine to osmotic release oral system- methylphenidate (OROS-MPH) was associated with improvements in selective areas of executive functioning, supporting the need for further research.
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Authors | Joseph Biederman, Ronna Fried, Laura Tarko, Craig Surman, Thomas Spencer, Amanda Pope, Rebecca Grossman, Katie McDermott, K Yvonne Woodworth, Stephen V Faraone |
Journal | Journal of attention disorders
(J Atten Disord)
Vol. 21
Issue 4
Pg. 343-352
(02 2017)
ISSN: 1557-1246 [Electronic] United States |
PMID | 24970718
(Publication Type: Comparative Study, Journal Article, Randomized Controlled Trial)
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Chemical References |
- Central Nervous System Stimulants
- Delayed-Action Preparations
- Methylphenidate
- Memantine
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Topics |
- Administration, Oral
- Adolescent
- Adult
- Attention Deficit Disorder with Hyperactivity
(drug therapy, psychology)
- Central Nervous System Stimulants
(administration & dosage, adverse effects)
- Delayed-Action Preparations
- Double-Blind Method
- Drug Therapy, Combination
- Executive Function
(drug effects)
- Female
- Humans
- Male
- Memantine
(administration & dosage, adverse effects)
- Methylphenidate
(administration & dosage, adverse effects)
- Middle Aged
- Osmosis
- Pilot Projects
- Treatment Outcome
- Young Adult
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