BENITIONSClinical Trial Intelligence

Comparative Effectiveness Research Trial for Antidepressant Incomplete and Non-responders With TRD

Фаза 4 Завершено NCT02977299

ЗаболеваниеTreatment Resistant Major Depressive Disorder
ФазаФаза 4
СпонсорMassachusetts General Hospital
СтатусЗавершено
Участники278 участн.
ВмешательствоAripiprazole, Repetitive transcranial magnetic stimulation (rTMS), Venlafaxine XR
Дата начала13.07.2017
Дата завершения24.04.2022
Публикация результатов9.07.2026

Кратко

This is a multi-site, randomized, open-label, effectiveness trial comparing three treatment arms for Major Depressive Disorder (MDD) patients with TRD who are currently on ongoing, stable and adequate antidepressant therapy (ADT). Adequate ADT is defined as a therapeutically sufficient dose for a sufficient treatment period, which would be expected to be effective as listed in the MGH Antidepressant Treatment Response Questionnaire (ATRQ). Patients will be randomized in a 1:1:1 fashion to one of three open-label treatment arms: a) aripiprazole augmentation, b) rTMS augmentation, and c) switching to venlafaxine XR or Duloxetine.

Montgomery-Asberg Depression Rating Scale (MADRS)

8 weeks · points

Aripiprazole Augmentation-14.9 ± 1.1 points
rTMS Augmentation-17.39 ± 1.3 points
Switch to Venlafaxine XR/Duloxetine-13.22 ± 1.1 points

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