The purpose of the study is to explore the efficacy and safety of H1-Coil deep brain rTMS in subjects with bipolar depression , currently treated with mood stabilizer and previously unsuccessfully treated with antidepressant medications
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
50
20 daily deep rTMS treatments
inactive treatment
shalvataMHC
Hod HaSharon, Israel
RECRUITINGchange in the Hamilton depression rating scale score
Time frame: 7 weeks
Clinical antidepressant remission at the end of the treatment, defined as exit Hamilton Depression Rating Scale <10.
Time frame: 7 weeks
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