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Efficacy and Safety of Transcranial Magnetic Stimulation in the Acute Treatment of Major Depression: A Multisite Randomized Controlled Trial

  • John P. O'Reardon
  • , H. Brent Solvason
  • , Philip G. Janicak
  • , Shirlene Sampson
  • , Keith E. Isenberg
  • , Ziad Nahas
  • , William M. McDonald
  • , David Avery
  • , Paul B. Fitzgerald
  • , Colleen Loo
  • , Mark A. Demitrack
  • , Mark S. George
  • , Harold A. Sackeim

Research output: Contribution to journal › Article › peer-review

Abstract

Background: We tested whether transcranial magnetic stimulation (TMS) over the left dorsolateral prefrontal cortex (DLPFC) is effective and safe in the acute treatment of major depression. Methods: In a double-blind, multisite study, 301 medication-free patients with major depression who had not benefited from prior treatment were randomized to active (n = 155) or sham TMS (n = 146) conditions. Sessions were conducted five times per week with TMS at 10 pulses/sec, 120% of motor threshold, 3000 pulses/session, for 4-6 weeks. Primary outcome was the symptom score change as assessed at week 4 with the Montgomery-Asberg Depression Rating Scale (MADRS). Secondary outcomes included changes on the 17- and 24-item Hamilton Depression Rating Scale (HAMD) and response and remission rates with the MADRS and HAMD. Results: Active TMS was significantly superior to sham TMS on the MADRS at week 4 (with a post hoc correction for inequality in symptom severity between groups at baseline), as well as on the HAMD17 and HAMD24 scales at weeks 4 and 6. Response rates were significantly higher with active TMS on all three scales at weeks 4 and 6. Remission rates were approximately twofold higher with active TMS at week 6 and significant on the MADRS and HAMD24 scales (but not the HAMD17 scale). Active TMS was well tolerated with a low dropout rate for adverse events (4.5%) that were generally mild and limited to transient scalp discomfort or pain. Conclusions: Transcranial magnetic stimulation was effective in treating major depression with minimal side effects reported. It offers clinicians a novel alternative for the treatment of this disorder.

Original languageEnglish (US)
Pages (from-to)1208-1216
Number of pages9
JournalBiological Psychiatry
Volume62
Issue number11
DOIs
StatePublished - Dec 1 2007

Bibliographical note

Funding Information:
Clinical trial is posted on www.clinicaltrials.gov . Listing No. NCT 00104611 . Supported by a grant from Neuronetics Inc.

Keywords

  • Clinical trial
  • TMS
  • efficacy
  • major depression
  • safety

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