The primary hypothesis of this confirmatory study is that lithium therapy will acutely decrease suicidal ideation and/or suicidal behaviour in inpatients with a major depressive episode (MDE, unipolar and bipolar disorder according to DSM IV criteria). The specific aim is to test the hypothesis that lithium plus treatment as usual (TAU), compared to placebo plus TAU, results in a significantly greater decrease in suicidal ideation and/or behaviour over 5 weeks in inpatients with MDE.
The study will consist of 254 adult patients, hospitalized for a major depressive episode with suicidal ideation and/or behaviour who will be randomized to two groups of each 127 participants. All study participants will receive treatment as usual in the hospital, including (psycho)pharmacological treatment and, if needed, psychotherapy plus a 5-week course of lithium or placebo. Rating scales will be used daily resp. weekly to measure suicidal ideation and/or behaviour, depression, anxiety, mixed/manic features and impulsiveness. Experienced clinicians will rate suicidal ideation and/or behaviour as well as depression twice a week and anxiety, mixed/manic features and impulsiveness once a week.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
254
Lithium as Add on to every necessary treatment as usual
Placebo as ADD-on to every necessary treatment as usual
Dept. of Psychiatry and Psychotherapy, Hospital of Dresden Neustadt
Dresden, Saxony, Germany
NOT_YET_RECRUITINGPsychiatrie, Verhaltensmedizin und Psychosomatik
Chemnitz, Germany
RECRUITINGKlinik für Psychiatrie, Psychosomatik und Psychotherapie Universitätsklinikum Frankfurt
Frankfurt am Main, Germany
RECRUITINGPsychatrie Universitätsmedizin Göttingen
Göttingen, Germany
RECRUITINGUniversitätsklinikum Heidelberg
Heidelberg, Germany
RECRUITINGS-STS
Change in the clinician administered (S-STS=Sheehan Suicidality Tracking Scale) total score between initial and final visit
Time frame: 5 Weeks
C-SSRS
Change of the total score of C-SSRS (Columbia-Suicide Severity Rating Scale) between start and final visit
Time frame: 5 weeks
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