Repetitive Versus Deep Transcranial Magnetic Stimulation for Major Depression
Major Depressive DisorderThe 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).
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Conditions de participation
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Sexe:
ALL -
Âges admissibles:
21 to 70
Critères de participation
Inclusion Criteria:
* Diagnosis of Major Depressive Disorder, at least moderate intensity, single or recurrent episode
* HRSD-17 score of at least 18
* No improvement to at least two adequate courses of antidepressants (based on the ATHF) or were unable to tolerate at least two separate trials of antidepressants of inadequate 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 received ECT or ketamine will be eligible to participate
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 the primary 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 least three months before entry into the study, with no anticipation of change
* Currently taking more than the equivalent of 2 mg of lorazepam of a benzodiazepine daily or any dose of an anticonvulsant due to the potential to limit TMS effectiveness
Lieu de l'étude
CHUM
CHUMMontréal, Quebec
Canada
Contactez l'équipe d'étude
Sylvie Tieu, B.Sc
Véronique Desbeaumes, Ph.D.
- Étude parrainée par
- Centre hospitalier de l'Université de Montréal (CHUM)
- Participants recherchés
- Plus d'informations
- ID de l'étude:
NCT05902312