The goal of this randomized controlled trial is to explore the efficacy and safety of two different dTMS devices in adolescent depression: deep TMS H1 coil and deep TMS H7 coil. The main questions it aims to answer are: Type of study: Clinical trial. Participant population: Adolescents with major depressive disorder (MDD). Objective: To explore whether the H7 coil is no less effective than the H1 coil for adolescents with MDD, further providing clinicians with additional treatment options for patients.
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Hamilton Depression Scale -24 (HAMD-24)
Timeframe: From enrollment to the end of treatment at 12 weeks
Response on Hamilton Depression Scale-24
Timeframe: From enrollment to the end of treatment at 12 weeks
Remission onHamilton Depression Scale-24
Timeframe: From enrollment to the end of treatment at 12 weeks