Repetitive Versus Deep Transcranial Magnetic Stimulation for Major Depression

Last updated: July 16, 2025
Sponsor: Centre hospitalier de l'Université de Montréal (CHUM)
Overall Status: Active - Not Recruiting

Phase

N/A

Condition

Depression (Major/severe)

Affective Disorders

Depression

Treatment

transcranial magnetic stimulation

Clinical Study ID

NCT05902312
2023-11389
  • Ages 21-70
  • All Genders

Study Summary

The goal of this randomized controlled trial is to he effectiveness of two different TMS techniques in TRD, repetitive TMS (rTMS) and deep TMS (dTMS). The main questions it aims to answer are:

type of study: clinical trial participant population/health conditions : Major Depressive Disorder To assess the superiority of dTMS over rTMS in TRD To evaluate the predictive capacity of scalable candidate biomarkers Participants will be randomly allocated to one of the two intervention groups (rTMS or dTMS).

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Diagnosis of Major Depressive Disorder, at least moderate intensity, single orrecurrent episode

  • HRSD-17 score of at least 18

  • No improvement to at least two adequate courses of antidepressants (based on theATHF) or were unable to tolerate at least two separate trials of antidepressants ofinadequate dose and duration

  • On a stable antidepressant regimen for the past four weeks before screening

  • Patients with a chronic depressive episode >2 years and who have previously receivedECT or ketamine will be eligible to participate

Exclusion

Exclusion Criteria:

  • Having previously received TMS;

  • Substance use disorder within the last three months

  • Diagnosis of bipolar or psychosis spectrum disorder

  • Anxiety or personality disorder that is assessed by a study investigator to be theprimary cause and causing greater impairment than MDD

  • Concomitant major unstable medical or neurological illness

  • Intracranial implant, cardiac pacemaker or implanted medication pump

  • Significant laboratory abnormality;

  • Active suicidal intent

  • Pregnancy

  • If participating in psychotherapy, must have been in stable treatment for at leastthree months before entry into the study, with no anticipation of change

  • Currently taking more than the equivalent of 2 mg of lorazepam of a benzodiazepinedaily or any dose of an anticonvulsant due to the potential to limit TMSeffectiveness

Study Design

Total Participants: 50
Treatment Group(s): 1
Primary Treatment: transcranial magnetic stimulation
Phase:
Study Start date:
January 01, 2024
Estimated Completion Date:
January 01, 2026

Study Description

The primary aim of this trial is to compare the effectiveness of two different TMS techniques in TRD, repetitive TMS (rTMS) and deep TMS (dTMS). Compared to rTMS, dTMS delivers a broader magnetic field, which in turn reduces coil positioning error and maximizes the probability of optimal cortical stimulation. A past RCT comparing both approaches found a greater depression score decrease and response/remission rates for dTMS, but was short of reaching significance for remission rates (primary outcome). Critical components of this RCT were suboptimal, including too few treatment sessions and insufficient statistical power, both of which could have obscured an actual difference between modalities. Proof of a more effective type of TMS over another would translate into increased odds of improvement for TRD patients who live with a chronic and disabling illness.

Connect with a study center

  • CHUM

    Montréal, Quebec H2X 0C1
    Canada

    Site Not Available

Not the study for you?

Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.