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Trial intelligence / Profile preview
NCT03043001Phase 3
Key facts
Phase 3, randomised, double-blind trial of memantine in bipolar disorder (BD) and alcohol dependence, sponsored by National Cheng Kung University Hospital. Primary endpoint: Change in plasma Brain-Derived Neurotropic Factor (BDNF) at week 12. Status: unknown.
add-on memantine therapy
Patients receive regular treatment with add-on memantine medication for 12 weeks.
Adults aged 18-65 with bipolar disorder and alcohol dependence, excluding pregnant/nursing women, those with poorly controlled medical conditions, or recent use of memantine, anti-inflammatories, or ECT.
Change in plasma Brain-Derived Neurotropic Factor (BDNF)
Change in attention
Change in side effects
Change in cytokine levels
Beyond the preview
Full results, competitive context and analysis are in the Gosset platform.
Available in the Gosset platform where reported.
Available in the Gosset platform where reported.
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