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Life sciences · Interventional Study
ClinicalTrials.gov · November 3, 2026
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Interventional Study.
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Registry record from ClinicalTrials.gov (NCT07369180). This is a study registration, not published results. Lead sponsor: NeuroQore Inc.. Recruitment status: COMPLETED. Phase: NA. Study type: INTERVENTIONAL. Enrollment: 56 participants (ACTUAL). Conditions: Major Depressive Disorder. Interventions: DEVICE: Active Accelerated rTMS Treatment; DEVICE: Sham Accelerated rTMS Treatment. Primary outcome measures: Change From Baseline in Montgomery-Åsberg Depression Rating Scale (MADRS) Total Score , Baseline (treatment day, pre-treatment), immediately post-treatment, 24 hours, 7 days and 30 days post-treatment. Brief summary: Transcranial Magnetic Stimulation (TMS) Therapy is a non-invasive procedure that uses magnetic pulses to stimulate the cortex (brain) to treat Major Depressive Disorder (MDD). Currently established therapy uses one 19-minute treatment session per day for 5 days per week for 6 weeks, for a total of 30 treatment sessions. The goal of this multi-site sham-controlled double-blinded randomized clinical trial is to evaluate the safety and effectiveness of accelerating the delivery of the NeuroQore Square TMS system's rectangular waveform rTMS protocol for the treatment of adults aged 22-85 with Major Depressive Disorder. The accelerated protocol of this study will involve the same currently FDA-cleared 19-min treatment session offered three times in a single day, with no additional treatment sessions.