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Keep this study
Lead
Tuscaloosa Research & Education Advancement Corporation
The primary objective of the study is to assess the long-term outcome in bipolar patients treated with divalproex versus lamotrigine in a retrospective chart review of veterans as measured by time to relapse into any significant mood episode (i.e. mania or depression). The primary hypothesis is that bipolar patients will demonstrate significantly greater time to relapse in those treated with divalproex compared to those treated with lamotrigine. The secondary objective of the study is to assess the safety and relative tolerability of divalproex and lamotrigine in this population based on discontinuation due to side or adverse effect.
Age
19–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Diagnosis of Bipolar I or Bipolar II disorder
Prescription of divalproex (any formulation except for Depakene/valproic acid) or lamotrigine in the electronic pharmacy profile.
Age 19 or older
Demonstrated stability for at least 4 weeks on an adequate dose of each medication (at least 50mg/d lamotrigine or 15mg/kg/day divalproex).
Treatment at the TVAMC for at least 6 months following the prescription of divalproex or lamotrigine.
You may not be if
Primary diagnosis of schizoaffective or schizophrenia during the evaluation period.
Prescription of divalproex and lamotrigine given concurrently during the observation period.
History of Dementia or cognitive disorders
Clareo Health | Divalproex vs. Lamotrigine for Bipolar Disorder
