Mood stabilizer treatment
Druglithium or valproate
Other names: lithium carbonate, Eskalith, Lithobid, divalproex sodium, Depakote, Depakene
NCT Number: NCT01272531
This is a prospective pharmacogenomics study of mood stabilizer response. The goal of this work is to identify genes associated with good response of patients with bipolar disorder to two commonly used mood stabilizing agents, lithium and valproate.
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Notify Me18 year and older
All sexes
Observational
Dalhousie University, Halifax, Nova Scotia, Canada
All subjects meeting study inclusion criteria will be started on lithium. Those that fail lithium will be crossed over to valproate (VPA). Those that also fail VPA will be again crossed-over to a standardized treatment as usual (TAU) arm. Subjects who are eligible for the study must be at least 18 years of age and have been diagnosed or are thought to have bipolar I disorder with at least one episode of mood instability in the last 12 months. They must also be eligible to take lithium and, if female and of child bearing age, agree to use adequate birth control methods and to inform their doctor of their plans to become pregnant.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
lithium or valproate
Other names: lithium carbonate, Eskalith, Lithobid, divalproex sodium, Depakote, Depakene
Time frame: every 2 months for 2 years
Relapse definition:
University of California, San Diego
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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