drugset / Trial / NCT00305578

Memantine Augmentation of Lamotrigine Incomplete-Response in Bipolar Depression

NCT00305578

Phase 4 Completed 29 enrolled Indiana University
RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of this study is to investigate whether addition of memantine to bipolar depression patients who have had an incomplete response to lamotrigine (Lamictal) which is frequently used to treat bipolar depression in the clinical setting. At present, memantine is approved for use in the treatment of Alzheimer's disease or dementia, but not for use for the treatment of bipolar depression. Subjects will be asked to participate because they are suffering from bipolar depression associated and have had an inadequate response to lamotrigine. Subjects will have to be on at least 100 mg per day, for at least 4 weeks.

Timeline

Start
2005-08
Primary completion
2010-12
Completion
2011-12

Drugs

EvaluationDrugModalityDoseRoute
Comparator Memantine Unknown 20 mg Oral

Indications