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This trial will compare the trajectories of improvement for three different patterns of twice-daily rTMS in major depression: two daily sessions of dorsomedial prefrontal rTMS delivered at 0 min vs. 30 min vs. 60 min intervals.
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Inclusion and exclusion criteria
Participants are eligible for the study if they:
Participants are ineligible for the study if they:
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180 participants in 3 patient groups
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Central trial contact
Laura Schulze; Terri Cairo
Data sourced from clinicaltrials.gov
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