A Double-Blind, Placebo-Controlled Study of Galantamine to Improve Cognitive Dysfunction in Bipolar Disorder
Completed · Phase 4 · Has a placebo group
Conditions studied: Bipolar Disorder
In brief
The purpose of this study is to determine if galantamine augmentaion improves cognition in euthymic bipolar patients. In addition, the effect of galantamine on clinical measures of functioning and psychopathology will also be assessed.
Key facts
- Study ID
- NCT00195845
- Run by
- Cambridge Health Alliance
- People needed
- 30
- Starts
- 2003-04-01
- Expected to finish
- 2007-02-01
- Last updated by the study team
- 2017-04-18
Who can join
Age: 18 and older, up to 60. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Age 18-60; DSM-IV diagnosis of bipolar disorder, any subtype; Baseline Mini Mental Status exam above 20; MRS < 16; MADRS < 16
You may not qualify if…
- Current substance dependence; serious unstable medical conditions; active suicidal ideation; current DSM-IV for a major mood episodes; history of COPD, epilepsy, cardiac arrhythmia, and peptic ulcer disease; meet DSM-IV criteria for dementia
Where it is running
- Cambridge Health Alliance — Cambridge, Massachusetts, United States
Full record on ClinicalTrials.gov
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